Canonical Allele Identifier: CA337955427

Gene: GABRD

Linked Data

• MyVariant Identifiers: chr1:g.1956418C>A (hg19) ; chr1:g.2024979C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2024979C>A , CM000663.2:g.2024979C>A	GRCh38
NC_000001.10:g.1956418C>A , CM000663.1:g.1956418C>A	GRCh37
NC_000001.9:g.1946278C>A	NCBI36
NG_008168.1:g.10651C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.106C>A MANE Select	ENSP00000367848.4:p.Leu36Met
ENST00000638411.1:c.106C>A	ENSP00000491632.1:p.Leu36Met
ENST00000638604.1:n.170C>A
ENST00000638771.1:c.106C>A	ENSP00000492435.1:p.Leu36Met
ENST00000639045.1:c.*92C>A	ENSP00000491997.1:n.*92C>A
ENST00000639777.1:n.710C>A
ENST00000639935.1:n.143C>A
ENST00000640030.1:c.46C>A	ENSP00000491411.1:p.Leu16Met
ENST00000640067.1:c.106C>A	ENSP00000491844.1:p.Leu36Met
ENST00000640423.1:n.115C>A
ENST00000640949.1:c.106C>A	ENSP00000492500.1:p.Leu36Met
ENST00000378585.5:c.106C>A	ENSP00000367848.4:p.Leu36Met
NM_000815.4:c.106C>A	NP_000806.2:p.Leu36Met
XM_011541194.1:c.145C>A	XP_011539496.1:p.Leu49Met
XM_011541194.3:c.145C>A	XP_011539496.1:p.Leu49Met
XM_017000936.1:c.811C>A	XP_016856425.1:p.Leu271Met
NM_000815.5:c.106C>A MANE Select	NP_000806.2:p.Leu36Met