Canonical Allele Identifier: CA812346926

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1354738588
• gnomAD v4: 5-56875399-A-T
• MyVariant Identifiers: chr5:g.56171226A>T (hg19) ; chr5:g.56875399A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875399A>T , CM000667.2:g.56875399A>T	GRCh38
NC_000005.9:g.56171226A>T , CM000667.1:g.56171226A>T	GRCh37
NC_000005.8:g.56206983A>T	NCBI36
NG_031884.1:g.65327A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1965+89A>T MANE Select	ENSP00000382423.3:n.1965+89A>T
ENST00000399503.3:c.1965+89A>T	ENSP00000382423.3:n.1965+89A>T
NM_005921.1:c.1965+89A>T	NP_005912.1:n.1965+89A>T
XM_005248519.3:c.1587+89A>T	XP_005248576.2:n.1587+89A>T
XM_011543406.1:c.1710+89A>T	XP_011541708.1:n.1710+89A>T
XM_011543407.1:c.1686+2394A>T	XP_011541709.1:n.1686+2394A>T
XM_011543408.1:c.1965+89A>T	XP_011541710.1:n.1965+89A>T
XM_017009484.1:c.1554+89A>T	XP_016864973.1:n.1554+89A>T
XM_017009485.1:c.1476+89A>T	XP_016864974.1:n.1476+89A>T
XR_001742068.2:n.1996+89A>T
NM_005921.2:c.1965+89A>T MANE Select	NP_005912.1:n.1965+89A>T