Canonical Allele Identifier: CA350780724
Gene: ERBB4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.212251734C>A (hg19) chr2:g.211387009C>A (hg38)
CIViC: CA350780724
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.211387009C>A , CM000664.2:g.211387009C>A GRCh38
NC_000002.11:g.212251734C>A , CM000664.1:g.212251734C>A GRCh37
NC_000002.10:g.211959979C>A NCBI36
NG_011805.1:g.1156619G>T
NG_011805.2:g.1156620G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260943.11:c.3247G>T ENSP00000260943.7:p.Gly1083Cys
ENST00000342788.9:c.3325G>T MANE Select ENSP00000342235.4:p.Gly1109Cys
ENST00000402597.6:c.3199G>T ENSP00000385565.3:p.Gly1067Cys
ENST00000342788.8:c.3325G>T ENSP00000342235.4:p.Gly1109Cys
ENST00000402597.5:c.3148G>T ENSP00000385565.2:p.Gly1050Cys
ENST00000436443.5:c.3277G>T ENSP00000403204.1:p.Gly1093Cys
NM_001042599.1:c.3277G>T NP_001036064.1:p.Gly1093Cys
NM_005235.2:c.3325G>T NP_005226.1:p.Gly1109Cys
XM_005246375.1:c.3322G>T XP_005246432.1:p.Gly1108Cys
XM_005246376.1:c.3295G>T XP_005246433.1:p.Gly1099Cys
XM_005246377.1:c.3247G>T XP_005246434.1:p.Gly1083Cys
XM_006712364.1:c.3370G>T XP_006712427.1:p.Gly1124Cys
XM_005246376.3:c.3295G>T XP_005246433.1:p.Gly1099Cys
XM_005246377.3:c.3247G>T XP_005246434.1:p.Gly1083Cys
XM_006712364.3:c.3370G>T XP_006712427.1:p.Gly1124Cys
XM_017003577.2:c.3448G>T XP_016859066.1:p.Gly1150Cys
XM_017003578.2:c.3403G>T XP_016859067.1:p.Gly1135Cys
XM_017003579.2:c.3400G>T XP_016859068.1:p.Gly1134Cys
XM_017003580.2:c.3373G>T XP_016859069.1:p.Gly1125Cys
XM_017003581.2:c.3355G>T XP_016859070.1:p.Gly1119Cys
XM_017003582.1:c.2749G>T XP_016859071.1:p.Gly917Cys
NM_005235.3:c.3325G>T MANE Select NP_005226.1:p.Gly1109Cys
Search 100 bp 5'
Search 100 bp 3'