Canonical Allele Identifier: CA359786362

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177704T>A (hg19) ; chr5:g.56881877T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881877T>A , CM000667.2:g.56881877T>A	GRCh38
NC_000005.9:g.56177704T>A , CM000667.1:g.56177704T>A	GRCh37
NC_000005.8:g.56213461T>A	NCBI36
NG_031884.1:g.71805T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2677T>A MANE Select	ENSP00000382423.3:p.Tyr893Asn
ENST00000399503.3:c.2677T>A	ENSP00000382423.3:p.Tyr893Asn
NM_005921.1:c.2677T>A	NP_005912.1:p.Tyr893Asn
XM_005248519.3:c.2299T>A	XP_005248576.2:p.Tyr767Asn
XM_011543406.1:c.2422T>A	XP_011541708.1:p.Tyr808Asn
XM_011543407.1:c.2398T>A	XP_011541709.1:p.Tyr800Asn
XM_011543408.1:c.2677T>A	XP_011541710.1:p.Tyr893Asn
XM_017009484.1:c.2266T>A	XP_016864973.1:p.Tyr756Asn
XM_017009485.1:c.2188T>A	XP_016864974.1:p.Tyr730Asn
XR_001742068.2:n.2708T>A
NM_005921.2:c.2677T>A MANE Select	NP_005912.1:p.Tyr893Asn