Canonical Allele Identifier: CA403380824
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs749615795
gnomAD v4: 19-4090638-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090638C>A , CM000681.2:g.4090638C>A GRCh38
NC_000019.9:g.4090636C>A , CM000681.1:g.4090636C>A GRCh37
NC_000019.8:g.4041636C>A NCBI36
NG_007996.1:g.38491G>T , LRG_750:g.38491G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1602G>T
ENST00000688002.1:n.3314G>T
ENST00000688751.1:n.299G>T
ENST00000689792.1:n.1067G>T
ENST00000262948.10:c.1163G>T MANE Select ENSP00000262948.4:p.Arg388Leu
ENST00000262948.9:c.1163G>T ENSP00000262948.3:p.Arg388Leu
ENST00000394867.8:c.872G>T ENSP00000378336.1:p.Arg291Leu
ENST00000597263.5:n.348G>T
ENST00000599021.1:c.273G>T
ENST00000600584.5:n.2612G>T
ENST00000601786.5:n.1464G>T
NM_030662.3:c.1163G>T , LRG_750t1:c.1163G>T NP_109587.1:p.Arg388Leu
XM_006722799.2:c.884G>T XP_006722862.1:p.Arg295Leu
XM_011528133.1:c.593G>T XP_011526435.1:p.Arg198Leu
NM_030662.4:c.1163G>T MANE Select NP_109587.1:p.Arg388Leu