Canonical Allele Identifier: CA337955470

Gene: GABRD

Linked Data

• MyVariant Identifiers: chr1:g.1956425T>A (hg19) ; chr1:g.2024986T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2024986T>A , CM000663.2:g.2024986T>A	GRCh38
NC_000001.10:g.1956425T>A , CM000663.1:g.1956425T>A	GRCh37
NC_000001.9:g.1946285T>A	NCBI36
NG_008168.1:g.10658T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.113T>A MANE Select	ENSP00000367848.4:p.Ile38Asn
ENST00000638411.1:c.113T>A	ENSP00000491632.1:p.Ile38Asn
ENST00000638604.1:n.177T>A
ENST00000638771.1:c.113T>A	ENSP00000492435.1:p.Ile38Asn
ENST00000639045.1:c.*99T>A	ENSP00000491997.1:n.*99T>A
ENST00000639777.1:n.717T>A
ENST00000639935.1:n.150T>A
ENST00000640030.1:c.53T>A	ENSP00000491411.1:p.Ile18Asn
ENST00000640067.1:c.113T>A	ENSP00000491844.1:p.Ile38Asn
ENST00000640423.1:n.122T>A
ENST00000640949.1:c.113T>A	ENSP00000492500.1:p.Ile38Asn
ENST00000378585.5:c.113T>A	ENSP00000367848.4:p.Ile38Asn
NM_000815.4:c.113T>A	NP_000806.2:p.Ile38Asn
XM_011541194.1:c.152T>A	XP_011539496.1:p.Ile51Asn
XM_011541194.3:c.152T>A	XP_011539496.1:p.Ile51Asn
XM_017000936.1:c.818T>A	XP_016856425.1:p.Ile273Asn
NM_000815.5:c.113T>A MANE Select	NP_000806.2:p.Ile38Asn