Canonical Allele Identifier: CA359787461

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111944716
• MyVariant Identifiers: chr5:g.56178037C>T (hg19) ; chr5:g.56882210C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882210C>T , CM000667.2:g.56882210C>T	GRCh38
NC_000005.9:g.56178037C>T , CM000667.1:g.56178037C>T	GRCh37
NC_000005.8:g.56213794C>T	NCBI36
NG_031884.1:g.72138C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3010C>T MANE Select	ENSP00000382423.3:p.His1004Tyr
ENST00000399503.3:c.3010C>T	ENSP00000382423.3:p.His1004Tyr
NM_005921.1:c.3010C>T	NP_005912.1:p.His1004Tyr
XM_005248519.3:c.2632C>T	XP_005248576.2:p.His878Tyr
XM_011543406.1:c.2755C>T	XP_011541708.1:p.His919Tyr
XM_011543407.1:c.2731C>T	XP_011541709.1:p.His911Tyr
XM_011543408.1:c.3010C>T	XP_011541710.1:p.His1004Tyr
XM_017009484.1:c.2599C>T	XP_016864973.1:p.His867Tyr
XM_017009485.1:c.2521C>T	XP_016864974.1:p.His841Tyr
XR_001742068.2:n.3041C>T
NM_005921.2:c.3010C>T MANE Select	NP_005912.1:p.His1004Tyr