Canonical Allele Identifier: CA359785650

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177398T>A (hg19) ; chr5:g.56881571T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881571T>A , CM000667.2:g.56881571T>A	GRCh38
NC_000005.9:g.56177398T>A , CM000667.1:g.56177398T>A	GRCh37
NC_000005.8:g.56213155T>A	NCBI36
NG_031884.1:g.71499T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2371T>A MANE Select	ENSP00000382423.3:p.Tyr791Asn
ENST00000399503.3:c.2371T>A	ENSP00000382423.3:p.Tyr791Asn
NM_005921.1:c.2371T>A	NP_005912.1:p.Tyr791Asn
XM_005248519.3:c.1993T>A	XP_005248576.2:p.Tyr665Asn
XM_011543406.1:c.2116T>A	XP_011541708.1:p.Tyr706Asn
XM_011543407.1:c.2092T>A	XP_011541709.1:p.Tyr698Asn
XM_011543408.1:c.2371T>A	XP_011541710.1:p.Tyr791Asn
XM_017009484.1:c.1960T>A	XP_016864973.1:p.Tyr654Asn
XM_017009485.1:c.1882T>A	XP_016864974.1:p.Tyr628Asn
XR_001742068.2:n.2402T>A
NM_005921.2:c.2371T>A MANE Select	NP_005912.1:p.Tyr791Asn