Canonical Allele Identifier: CA2211806226

Gene: GPR139

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.20049508C= , CM000678.2:g.20049508C=	GRCh38
NC_000016.9:g.20060830C= , CM000678.1:g.20060830C=	GRCh37
NC_000016.8:g.19968331C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001002911.4:c.128-16839G= MANE Select	NP_001002911.1:n.128-16839G=
ENST00000570682.2:c.128-16839G= MANE Select	ENSP00000458791.2:n.128-16839G=
NM_001002911.2:c.128-16839G=	NP_001002911.1:n.128-16839G=
NM_001002911.3:c.128-16839G=	NP_001002911.1:n.128-16839G=
NM_001318483.1:c.-152-16839G=	NP_001305412.1:n.-152-16839G=
ENST00000326571.7:c.*74-16839G=	ENSP00000370779.5:n.*74-16839G=
ENST00000570682.1:c.128-16839G=	ENSP00000458791.1:n.128-16839G=
XM_005255114.2:c.-152-16839G=	XP_005255171.1:n.-152-16839G=