Canonical Allele Identifier: CA504984328
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090646-T-C
MyVariant Identifiers: chr19:g.4090644T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090646T>C , CM000681.2:g.4090646T>C GRCh38
NC_000019.9:g.4090644T>C , CM000681.1:g.4090644T>C GRCh37
NC_000019.8:g.4041644T>C NCBI36
NG_007996.1:g.38483A>G , LRG_750:g.38483A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1594A>G
ENST00000688002.1:n.3306A>G
ENST00000688751.1:n.291A>G
ENST00000689792.1:n.1059A>G
ENST00000262948.10:c.1155A>G MANE Select ENSP00000262948.4:p.Lys385=
ENST00000262948.9:c.1155A>G ENSP00000262948.3:p.Lys385=
ENST00000394867.8:c.864A>G ENSP00000378336.1:p.Lys288=
ENST00000597263.5:n.340A>G
ENST00000599021.1:c.265A>G
ENST00000600584.5:n.2604A>G
ENST00000601786.5:n.1456A>G
NM_030662.3:c.1155A>G , LRG_750t1:c.1155A>G NP_109587.1:p.Lys385=
XM_006722799.2:c.876A>G XP_006722862.1:p.Lys292=
XM_011528133.1:c.585A>G XP_011526435.1:p.Lys195=
NM_030662.4:c.1155A>G MANE Select NP_109587.1:p.Lys385=