Canonical Allele Identifier: CA714067

Gene: MAP3K6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.27364279A>C , CM000663.2:g.27364279A>C	GRCh38
NC_000001.10:g.27690770A>C , CM000663.1:g.27690770A>C	GRCh37
NC_000001.9:g.27563357A>C	NCBI36
NG_051309.1:g.8759T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004672.5:c.620T>G MANE Select	NP_004663.3:p.Val207Gly
ENST00000357582.3:c.620T>G MANE Select	ENSP00000350195.2:p.Val207Gly
NM_001297609.1:c.596T>G	NP_001284538.1:p.Val199Gly
NM_001297609.2:c.596T>G	NP_001284538.1:p.Val199Gly
NM_004672.4:c.620T>G	NP_004663.3:p.Val207Gly
ENST00000357582.2:c.620T>G	ENSP00000350195.2:p.Val207Gly
ENST00000374040.7:c.596T>G	ENSP00000363152.2:p.Val199Gly
ENST00000493901.5:c.620T>G	ENSP00000419591.1:p.Val207Gly
ENST00000493901.6:n.224T>G
XM_011542406.1:c.620T>G	XP_011540708.1:p.Val207Gly
XM_017002771.1:c.-650T>G	XP_016858260.1:n.-650T>G
XM_017002772.1:c.620T>G	XP_016858261.1:p.Val207Gly
XR_241205.3:n.2037T>G
XR_946794.1:n.2022T>G
XR_946794.3:n.2051T>G
XR_946795.1:n.2022T>G
XR_946795.3:n.2050T>G