Canonical Allele Identifier: CA504984320
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090637-C-A
MyVariant Identifiers: chr19:g.4090635C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090637C>A , CM000681.2:g.4090637C>A GRCh38
NC_000019.9:g.4090635C>A , CM000681.1:g.4090635C>A GRCh37
NC_000019.8:g.4041635C>A NCBI36
NG_007996.1:g.38492G>T , LRG_750:g.38492G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1603G>T
ENST00000688002.1:n.3315G>T
ENST00000688751.1:n.300G>T
ENST00000689792.1:n.1068G>T
ENST00000262948.10:c.1164G>T MANE Select ENSP00000262948.4:p.Arg388=
ENST00000262948.9:c.1164G>T ENSP00000262948.3:p.Arg388=
ENST00000394867.8:c.873G>T ENSP00000378336.1:p.Arg291=
ENST00000597263.5:n.349G>T
ENST00000599021.1:c.274G>T
ENST00000600584.5:n.2613G>T
ENST00000601786.5:n.1465G>T
NM_030662.3:c.1164G>T , LRG_750t1:c.1164G>T NP_109587.1:p.Arg388=
XM_006722799.2:c.885G>T XP_006722862.1:p.Arg295=
XM_011528133.1:c.594G>T XP_011526435.1:p.Arg198=
NM_030662.4:c.1164G>T MANE Select NP_109587.1:p.Arg388=