Canonical Allele Identifier: CA359785925

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177525T>C (hg19) ; chr5:g.56881698T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881698T>C , CM000667.2:g.56881698T>C	GRCh38
NC_000005.9:g.56177525T>C , CM000667.1:g.56177525T>C	GRCh37
NC_000005.8:g.56213282T>C	NCBI36
NG_031884.1:g.71626T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2498T>C MANE Select	ENSP00000382423.3:p.Val833Ala
ENST00000399503.3:c.2498T>C	ENSP00000382423.3:p.Val833Ala
NM_005921.1:c.2498T>C	NP_005912.1:p.Val833Ala
XM_005248519.3:c.2120T>C	XP_005248576.2:p.Val707Ala
XM_011543406.1:c.2243T>C	XP_011541708.1:p.Val748Ala
XM_011543407.1:c.2219T>C	XP_011541709.1:p.Val740Ala
XM_011543408.1:c.2498T>C	XP_011541710.1:p.Val833Ala
XM_017009484.1:c.2087T>C	XP_016864973.1:p.Val696Ala
XM_017009485.1:c.2009T>C	XP_016864974.1:p.Val670Ala
XR_001742068.2:n.2529T>C
NM_005921.2:c.2498T>C MANE Select	NP_005912.1:p.Val833Ala