Canonical Allele Identifier: CA359802480

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1747449184
• gnomAD v3: 5-56859794-C-A
• gnomAD v4: 5-56859794-C-A
• MyVariant Identifiers: chr5:g.56155621C>A (hg19) ; chr5:g.56859794C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859794C>A , CM000667.2:g.56859794C>A	GRCh38
NC_000005.9:g.56155621C>A , CM000667.1:g.56155621C>A	GRCh37
NC_000005.8:g.56191378C>A	NCBI36
NG_031884.1:g.49722C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.713C>A MANE Select	ENSP00000382423.3:p.Ala238Glu
ENST00000399503.3:c.713C>A	ENSP00000382423.3:p.Ala238Glu
NM_005921.1:c.713C>A	NP_005912.1:p.Ala238Glu
XM_005248519.3:c.335C>A	XP_005248576.2:p.Ala112Glu
XM_011543406.1:c.458C>A	XP_011541708.1:p.Ala153Glu
XM_011543407.1:c.713C>A	XP_011541709.1:p.Ala238Glu
XM_011543408.1:c.713C>A	XP_011541710.1:p.Ala238Glu
XM_017009484.1:c.302C>A	XP_016864973.1:p.Ala101Glu
XM_017009485.1:c.224C>A	XP_016864974.1:p.Ala75Glu
XR_001742068.2:n.744C>A
NM_005921.2:c.713C>A MANE Select	NP_005912.1:p.Ala238Glu