Canonical Allele Identifier: CA415448464

Gene: GABRD

Linked Data

• MyVariant Identifiers: chr1:g.1956483T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2025044T>G , CM000663.2:g.2025044T>G	GRCh38
NC_000001.10:g.1956483T>G , CM000663.1:g.1956483T>G	GRCh37
NC_000001.9:g.1946343T>G	NCBI36
NG_008168.1:g.10716T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.171T>G MANE Select	ENSP00000367848.4:p.Pro57=
ENST00000638411.1:c.171T>G	ENSP00000491632.1:p.Pro57=
ENST00000638604.1:n.235T>G
ENST00000638771.1:c.171T>G	ENSP00000492435.1:p.Pro57=
ENST00000639045.1:c.*157T>G	ENSP00000491997.1:n.*157T>G
ENST00000639777.1:n.775T>G
ENST00000639935.1:n.208T>G
ENST00000640030.1:c.111T>G	ENSP00000491411.1:p.Pro37=
ENST00000640067.1:c.171T>G	ENSP00000491844.1:p.Pro57=
ENST00000640423.1:n.180T>G
ENST00000640949.1:c.171T>G	ENSP00000492500.1:p.Pro57=
ENST00000378585.5:c.171T>G	ENSP00000367848.4:p.Pro57=
NM_000815.4:c.171T>G	NP_000806.2:p.Pro57=
XM_011541194.1:c.210T>G	XP_011539496.1:p.Pro70=
XM_011541194.3:c.210T>G	XP_011539496.1:p.Pro70=
XM_017000936.1:c.876T>G	XP_016856425.1:p.Pro292=
NM_000815.5:c.171T>G MANE Select	NP_000806.2:p.Pro57=