Canonical Allele Identifier: CA415448360

Gene: GABRD

Linked Data

• MyVariant Identifiers: chr1:g.1956456A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2025017A>C , CM000663.2:g.2025017A>C	GRCh38
NC_000001.10:g.1956456A>C , CM000663.1:g.1956456A>C	GRCh37
NC_000001.9:g.1946316A>C	NCBI36
NG_008168.1:g.10689A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.144A>C MANE Select	ENSP00000367848.4:p.Ile48=
ENST00000638411.1:c.144A>C	ENSP00000491632.1:p.Ile48=
ENST00000638604.1:n.208A>C
ENST00000638771.1:c.144A>C	ENSP00000492435.1:p.Ile48=
ENST00000639045.1:c.*130A>C	ENSP00000491997.1:n.*130A>C
ENST00000639777.1:n.748A>C
ENST00000639935.1:n.181A>C
ENST00000640030.1:c.84A>C	ENSP00000491411.1:p.Ile28=
ENST00000640067.1:c.144A>C	ENSP00000491844.1:p.Ile48=
ENST00000640423.1:n.153A>C
ENST00000640949.1:c.144A>C	ENSP00000492500.1:p.Ile48=
ENST00000378585.5:c.144A>C	ENSP00000367848.4:p.Ile48=
NM_000815.4:c.144A>C	NP_000806.2:p.Ile48=
XM_011541194.1:c.183A>C	XP_011539496.1:p.Ile61=
XM_011541194.3:c.183A>C	XP_011539496.1:p.Ile61=
XM_017000936.1:c.849A>C	XP_016856425.1:p.Ile283=
NM_000815.5:c.144A>C MANE Select	NP_000806.2:p.Ile48=