Canonical Allele Identifier: CA1290487332

Gene: MAP3K19

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135045855G= , CM000664.2:g.135045855G=	GRCh38
NC_000002.11:g.135803425G= , CM000664.1:g.135803425G=	GRCh37
NC_000002.10:g.135519895G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392915.7:c.-424+1330C= MANE Select	ENSP00000376647.2:n.-424+1330C=
ENST00000392915.6:c.-424+1330C=	ENSP00000376647.2:n.-424+1330C=
ENST00000486077.2:n.260+1330C=
ENST00000637841.1:c.-288+1330C=	ENSP00000489676.1:n.-288+1330C=
ENST00000414343.1:c.-203+1330C=	ENSP00000416345.1:n.-203+1330C=
ENST00000468155.5:n.284+1330C=
ENST00000486077.1:n.259+1330C=
XM_011511892.1:c.-480+1330C=	XP_011510194.1:n.-480+1330C=
XM_017005003.1:c.-424+1330C=	XP_016860492.1:n.-424+1330C=
XM_017005004.2:c.-392+1330C=	XP_016860493.1:n.-392+1330C=
XM_017005005.2:c.-203+1330C=	XP_016860494.1:n.-203+1330C=
NM_025052.5:c.-424+1330C= MANE Select	NP_079328.3:n.-424+1330C=
NM_001400438.1:c.-480+1330C=	NP_001387367.1:n.-480+1330C=