Canonical Allele Identifier: CA359787417

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1446404328
• MyVariant Identifiers: chr5:g.56178016A>T (hg19) ; chr5:g.56882189A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882189A>T , CM000667.2:g.56882189A>T	GRCh38
NC_000005.9:g.56178016A>T , CM000667.1:g.56178016A>T	GRCh37
NC_000005.8:g.56213773A>T	NCBI36
NG_031884.1:g.72117A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2989A>T MANE Select	ENSP00000382423.3:p.Thr997Ser
ENST00000399503.3:c.2989A>T	ENSP00000382423.3:p.Thr997Ser
NM_005921.1:c.2989A>T	NP_005912.1:p.Thr997Ser
XM_005248519.3:c.2611A>T	XP_005248576.2:p.Thr871Ser
XM_011543406.1:c.2734A>T	XP_011541708.1:p.Thr912Ser
XM_011543407.1:c.2710A>T	XP_011541709.1:p.Thr904Ser
XM_011543408.1:c.2989A>T	XP_011541710.1:p.Thr997Ser
XM_017009484.1:c.2578A>T	XP_016864973.1:p.Thr860Ser
XM_017009485.1:c.2500A>T	XP_016864974.1:p.Thr834Ser
XR_001742068.2:n.3020A>T
NM_005921.2:c.2989A>T MANE Select	NP_005912.1:p.Thr997Ser