Canonical Allele Identifier: CA1149430214

Gene: GABRD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2025049T= , CM000663.2:g.2025049T=	GRCh38
NC_000001.10:g.1956488T= , CM000663.1:g.1956488T=	GRCh37
NC_000001.9:g.1946348T=	NCBI36
NG_008168.1:g.10721T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.176T= MANE Select	ENSP00000367848.4:p.Ile59=
ENST00000638411.1:c.176T=	ENSP00000491632.1:p.Ile59=
ENST00000638604.1:n.240T=
ENST00000638771.1:c.176T=	ENSP00000492435.1:p.Ile59=
ENST00000639045.1:c.*162T=	ENSP00000491997.1:n.*162T=
ENST00000639777.1:n.780T=
ENST00000639935.1:n.213T=
ENST00000640030.1:c.116T=	ENSP00000491411.1:p.Ile39=
ENST00000640067.1:c.176T=	ENSP00000491844.1:p.Ile59=
ENST00000640423.1:n.185T=
ENST00000640949.1:c.176T=	ENSP00000492500.1:p.Ile59=
ENST00000378585.5:c.176T=	ENSP00000367848.4:p.Ile59=
NM_000815.4:c.176T=	NP_000806.2:p.Ile59=
XM_011541194.1:c.215T=	XP_011539496.1:p.Ile72=
XM_011541194.3:c.215T=	XP_011539496.1:p.Ile72=
XM_017000936.1:c.881T=	XP_016856425.1:p.Ile294=
NM_000815.5:c.176T= MANE Select	NP_000806.2:p.Ile59=