Canonical Allele Identifier: CA504984340
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090670-C-A
MyVariant Identifiers: chr19:g.4090668C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090670C>A , CM000681.2:g.4090670C>A GRCh38
NC_000019.9:g.4090668C>A , CM000681.1:g.4090668C>A GRCh37
NC_000019.8:g.4041668C>A NCBI36
NG_007996.1:g.38459G>T , LRG_750:g.38459G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1570G>T
ENST00000688002.1:n.3282G>T
ENST00000688751.1:n.267G>T
ENST00000689792.1:n.1035G>T
ENST00000262948.10:c.1131G>T MANE Select ENSP00000262948.4:p.Val377=
ENST00000262948.9:c.1131G>T ENSP00000262948.3:p.Val377=
ENST00000394867.8:c.840G>T ENSP00000378336.1:p.Val280=
ENST00000597263.5:n.316G>T
ENST00000599021.1:c.241G>T
ENST00000600584.5:n.2580G>T
ENST00000601786.5:n.1432G>T
NM_030662.3:c.1131G>T , LRG_750t1:c.1131G>T NP_109587.1:p.Val377=
XM_006722799.2:c.852G>T XP_006722862.1:p.Val284=
XM_011528133.1:c.561G>T XP_011526435.1:p.Val187=
NM_030662.4:c.1131G>T MANE Select NP_109587.1:p.Val377=