Canonical Allele Identifier: CA359781032

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111921243
• MyVariant Identifiers: chr5:g.56171025C>T (hg19) ; chr5:g.56875198C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875198C>T , CM000667.2:g.56875198C>T	GRCh38
NC_000005.9:g.56171025C>T , CM000667.1:g.56171025C>T	GRCh37
NC_000005.8:g.56206782C>T	NCBI36
NG_031884.1:g.65126C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1853C>T MANE Select	ENSP00000382423.3:p.Ala618Val
ENST00000399503.3:c.1853C>T	ENSP00000382423.3:p.Ala618Val
NM_005921.1:c.1853C>T	NP_005912.1:p.Ala618Val
XM_005248519.3:c.1475C>T	XP_005248576.2:p.Ala492Val
XM_011543406.1:c.1598C>T	XP_011541708.1:p.Ala533Val
XM_011543407.1:c.1686+2193C>T	XP_011541709.1:n.1686+2193C>T
XM_011543408.1:c.1853C>T	XP_011541710.1:p.Ala618Val
XM_017009484.1:c.1442C>T	XP_016864973.1:p.Ala481Val
XM_017009485.1:c.1364C>T	XP_016864974.1:p.Ala455Val
XR_001742068.2:n.1884C>T
NM_005921.2:c.1853C>T MANE Select	NP_005912.1:p.Ala618Val