Canonical Allele Identifier: CA713855

Gene: MAP3K6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.27362714T>C , CM000663.2:g.27362714T>C	GRCh38
NC_000001.10:g.27689205T>C , CM000663.1:g.27689205T>C	GRCh37
NC_000001.9:g.27561792T>C	NCBI36
NG_051309.1:g.10324A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357582.3:c.1182A>G MANE Select	ENSP00000350195.2:p.Ser394=
ENST00000493901.6:n.786A>G
ENST00000671291.1:n.16A>G
ENST00000357582.2:c.1182A>G	ENSP00000350195.2:p.Ser394=
ENST00000374040.7:c.1158A>G	ENSP00000363152.2:p.Ser386=
ENST00000472410.5:c.353A>G
ENST00000493901.5:c.1182A>G	ENSP00000419591.1:p.Ser394=
NM_001297609.1:c.1158A>G	NP_001284538.1:p.Ser386=
NM_004672.4:c.1182A>G	NP_004663.3:p.Ser394=
XM_011542406.1:c.1182A>G	XP_011540708.1:p.Ser394=
XR_241205.3:n.2599A>G
XR_946794.1:n.2584A>G
XR_946795.1:n.2584A>G
XM_017002771.1:c.-76A>G	XP_016858260.1:n.-76A>G
XM_017002772.1:c.1182A>G	XP_016858261.1:p.Ser394=
XR_946794.3:n.2613A>G
XR_946795.3:n.2612A>G
NM_004672.5:c.1182A>G MANE Select	NP_004663.3:p.Ser394=
NM_001297609.2:c.1158A>G	NP_001284538.1:p.Ser386=