Canonical Allele Identifier: CA2673909927

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56881451-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881451T>A , CM000667.2:g.56881451T>A	GRCh38
NC_000005.9:g.56177278T>A , CM000667.1:g.56177278T>A	GRCh37
NC_000005.8:g.56213035T>A	NCBI36
NG_031884.1:g.71379T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2370-119T>A MANE Select	ENSP00000382423.3:n.2370-119T>A
ENST00000399503.3:c.2370-119T>A	ENSP00000382423.3:n.2370-119T>A
NM_005921.1:c.2370-119T>A	NP_005912.1:n.2370-119T>A
XM_005248519.3:c.1992-119T>A	XP_005248576.2:n.1992-119T>A
XM_011543406.1:c.2115-119T>A	XP_011541708.1:n.2115-119T>A
XM_011543407.1:c.2091-119T>A	XP_011541709.1:n.2091-119T>A
XM_011543408.1:c.2370-119T>A	XP_011541710.1:n.2370-119T>A
XM_017009484.1:c.1959-119T>A	XP_016864973.1:n.1959-119T>A
XM_017009485.1:c.1881-119T>A	XP_016864974.1:n.1881-119T>A
XR_001742068.2:n.2401-119T>A
NM_005921.2:c.2370-119T>A MANE Select	NP_005912.1:n.2370-119T>A