Canonical Allele Identifier: CA359787817

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178199C>T (hg19) ; chr5:g.56882372C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882372C>T , CM000667.2:g.56882372C>T	GRCh38
NC_000005.9:g.56178199C>T , CM000667.1:g.56178199C>T	GRCh37
NC_000005.8:g.56213956C>T	NCBI36
NG_031884.1:g.72300C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3172C>T MANE Select	ENSP00000382423.3:p.His1058Tyr
ENST00000399503.3:c.3172C>T	ENSP00000382423.3:p.His1058Tyr
NM_005921.1:c.3172C>T	NP_005912.1:p.His1058Tyr
XM_005248519.3:c.2794C>T	XP_005248576.2:p.His932Tyr
XM_011543406.1:c.2917C>T	XP_011541708.1:p.His973Tyr
XM_011543407.1:c.2893C>T	XP_011541709.1:p.His965Tyr
XM_011543408.1:c.3172C>T	XP_011541710.1:p.His1058Tyr
XM_017009484.1:c.2761C>T	XP_016864973.1:p.His921Tyr
XM_017009485.1:c.2683C>T	XP_016864974.1:p.His895Tyr
XR_001742068.2:n.3203C>T
NM_005921.2:c.3172C>T MANE Select	NP_005912.1:p.His1058Tyr