Canonical Allele Identifier: CA3273019

Gene: MAP3K1

Linked Data

• dbSNP Id: rs768180463
• ExAC: 5:56177585 G / A
• gnomAD v2: 5-56177585-G-A
• gnomAD v3: 5-56881758-G-A
• gnomAD v4: 5-56881758-G-A
• MyVariant Identifiers: chr5:g.56177585G>A (hg19) ; chr5:g.56881758G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881758G>A , CM000667.2:g.56881758G>A	GRCh38
NC_000005.9:g.56177585G>A , CM000667.1:g.56177585G>A	GRCh37
NC_000005.8:g.56213342G>A	NCBI36
NG_031884.1:g.71686G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2558G>A MANE Select	ENSP00000382423.3:p.Arg853His
ENST00000399503.3:c.2558G>A	ENSP00000382423.3:p.Arg853His
NM_005921.1:c.2558G>A	NP_005912.1:p.Arg853His
XM_005248519.3:c.2180G>A	XP_005248576.2:p.Arg727His
XM_011543406.1:c.2303G>A	XP_011541708.1:p.Arg768His
XM_011543407.1:c.2279G>A	XP_011541709.1:p.Arg760His
XM_011543408.1:c.2558G>A	XP_011541710.1:p.Arg853His
XM_017009484.1:c.2147G>A	XP_016864973.1:p.Arg716His
XM_017009485.1:c.2069G>A	XP_016864974.1:p.Arg690His
XR_001742068.2:n.2589G>A
NM_005921.2:c.2558G>A MANE Select	NP_005912.1:p.Arg853His