Canonical Allele Identifier: CA359802659

Gene: MAP3K1

Linked Data

• dbSNP Id: rs974500601
• MyVariant Identifiers: chr5:g.56155713G>C (hg19) ; chr5:g.56859886G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859886G>C , CM000667.2:g.56859886G>C	GRCh38
NC_000005.9:g.56155713G>C , CM000667.1:g.56155713G>C	GRCh37
NC_000005.8:g.56191470G>C	NCBI36
NG_031884.1:g.49814G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.805G>C MANE Select	ENSP00000382423.3:p.Val269Leu
ENST00000399503.3:c.805G>C	ENSP00000382423.3:p.Val269Leu
NM_005921.1:c.805G>C	NP_005912.1:p.Val269Leu
XM_005248519.3:c.427G>C	XP_005248576.2:p.Val143Leu
XM_011543406.1:c.550G>C	XP_011541708.1:p.Val184Leu
XM_011543407.1:c.805G>C	XP_011541709.1:p.Val269Leu
XM_011543408.1:c.805G>C	XP_011541710.1:p.Val269Leu
XM_017009484.1:c.394G>C	XP_016864973.1:p.Val132Leu
XM_017009485.1:c.316G>C	XP_016864974.1:p.Val106Leu
XR_001742068.2:n.836G>C
NM_005921.2:c.805G>C MANE Select	NP_005912.1:p.Val269Leu