Canonical Allele Identifier: CA359785652

Gene: MAP3K1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2371T>G MANE Select	ENSP00000382423.3:p.Tyr791Asp
ENST00000399503.3:c.2371T>G	ENSP00000382423.3:p.Tyr791Asp
NM_005921.1:c.2371T>G	NP_005912.1:p.Tyr791Asp
XM_005248519.3:c.1993T>G	XP_005248576.2:p.Tyr665Asp
XM_011543406.1:c.2116T>G	XP_011541708.1:p.Tyr706Asp
XM_011543407.1:c.2092T>G	XP_011541709.1:p.Tyr698Asp
XM_011543408.1:c.2371T>G	XP_011541710.1:p.Tyr791Asp
XM_017009484.1:c.1960T>G	XP_016864973.1:p.Tyr654Asp
XM_017009485.1:c.1882T>G	XP_016864974.1:p.Tyr628Asp
XR_001742068.2:n.2402T>G
NM_005921.2:c.2371T>G MANE Select	NP_005912.1:p.Tyr791Asp