Canonical Allele Identifier: CA812363615

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1254911205
• MyVariant Identifiers: chr5:g.56153314T>C (hg19) ; chr5:g.56857487T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56857487T>C , CM000667.2:g.56857487T>C	GRCh38
NC_000005.9:g.56153314T>C , CM000667.1:g.56153314T>C	GRCh37
NC_000005.8:g.56189071T>C	NCBI36
NG_031884.1:g.47415T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.633+737T>C MANE Select	ENSP00000382423.3:n.633+737T>C
ENST00000399503.3:c.633+737T>C	ENSP00000382423.3:n.633+737T>C
NM_005921.1:c.633+737T>C	NP_005912.1:n.633+737T>C
XM_005248519.3:c.255+737T>C	XP_005248576.2:n.255+737T>C
XM_011543406.1:c.378+737T>C	XP_011541708.1:n.378+737T>C
XM_011543407.1:c.633+737T>C	XP_011541709.1:n.633+737T>C
XM_011543408.1:c.633+737T>C	XP_011541710.1:n.633+737T>C
XM_017009484.1:c.222+737T>C	XP_016864973.1:n.222+737T>C
XM_017009485.1:c.144+737T>C	XP_016864974.1:n.144+737T>C
XR_001742068.2:n.664+737T>C
NM_005921.2:c.633+737T>C MANE Select	NP_005912.1:n.633+737T>C