Canonical Allele Identifier: CA359786378

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177706T>A (hg19) ; chr5:g.56881879T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881879T>A , CM000667.2:g.56881879T>A	GRCh38
NC_000005.9:g.56177706T>A , CM000667.1:g.56177706T>A	GRCh37
NC_000005.8:g.56213463T>A	NCBI36
NG_031884.1:g.71807T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2679T>A MANE Select	ENSP00000382423.3:p.Tyr893Ter
ENST00000399503.3:c.2679T>A	ENSP00000382423.3:p.Tyr893Ter
NM_005921.1:c.2679T>A	NP_005912.1:p.Tyr893Ter
XM_005248519.3:c.2301T>A	XP_005248576.2:p.Tyr767Ter
XM_011543406.1:c.2424T>A	XP_011541708.1:p.Tyr808Ter
XM_011543407.1:c.2400T>A	XP_011541709.1:p.Tyr800Ter
XM_011543408.1:c.2679T>A	XP_011541710.1:p.Tyr893Ter
XM_017009484.1:c.2268T>A	XP_016864973.1:p.Tyr756Ter
XM_017009485.1:c.2190T>A	XP_016864974.1:p.Tyr730Ter
XR_001742068.2:n.2710T>A
NM_005921.2:c.2679T>A MANE Select	NP_005912.1:p.Tyr893Ter