Canonical Allele Identifier: CA1645344040

Gene: GABRR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.89217256C= , CM000668.2:g.89217256C=	GRCh38
NC_000006.11:g.89926975C= , CM000668.1:g.89926975C=	GRCh37
NC_000006.10:g.89983694C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000454853.7:c.67G= MANE Select	ENSP00000412673.2:p.Glu23=
ENST00000369451.7:c.-239+4019G=	ENSP00000358463.3:n.-239+4019G=
ENST00000435811.5:c.67G=	ENSP00000394687.1:p.Glu23=
ENST00000454853.6:c.67G=	ENSP00000412673.2:p.Glu23=
ENST00000457434.1:c.67G=	ENSP00000410130.1:p.Glu23=
ENST00000481493.1:n.6G=
ENST00000611484.4:c.-297G=	ENSP00000478846.1:n.-297G=
ENST00000621627.4:c.-242+4019G=	ENSP00000481986.1:n.-242+4019G=
NM_001256703.1:c.67G=	NP_001243632.1:p.Glu23=
NM_001256704.1:c.-297G=	NP_001243633.1:n.-297G=
NM_001267582.1:c.-242+4019G=	NP_001254511.1:n.-242+4019G=
NM_002042.4:c.67G=	NP_002033.2:p.Glu23=
XM_006715438.2:c.67G=	XP_006715501.1:p.Glu23=
XM_017010689.1:c.-294G=	XP_016866178.1:n.-294G=
NM_002042.5:c.67G= MANE Select	NP_002033.2:p.Glu23=
NM_001267582.2:c.-242+4019G=	NP_001254511.1:n.-242+4019G=