Canonical Allele Identifier: CA359802592

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155680T>A (hg19) ; chr5:g.56859853T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859853T>A , CM000667.2:g.56859853T>A	GRCh38
NC_000005.9:g.56155680T>A , CM000667.1:g.56155680T>A	GRCh37
NC_000005.8:g.56191437T>A	NCBI36
NG_031884.1:g.49781T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.772T>A MANE Select	ENSP00000382423.3:p.Ser258Thr
ENST00000399503.3:c.772T>A	ENSP00000382423.3:p.Ser258Thr
NM_005921.1:c.772T>A	NP_005912.1:p.Ser258Thr
XM_005248519.3:c.394T>A	XP_005248576.2:p.Ser132Thr
XM_011543406.1:c.517T>A	XP_011541708.1:p.Ser173Thr
XM_011543407.1:c.772T>A	XP_011541709.1:p.Ser258Thr
XM_011543408.1:c.772T>A	XP_011541710.1:p.Ser258Thr
XM_017009484.1:c.361T>A	XP_016864973.1:p.Ser121Thr
XM_017009485.1:c.283T>A	XP_016864974.1:p.Ser95Thr
XR_001742068.2:n.803T>A
NM_005921.2:c.772T>A MANE Select	NP_005912.1:p.Ser258Thr