Canonical Allele Identifier: CA337955323

Gene: GABRD

Linked Data

• gnomAD v4: 1-2024966-C-G
• MyVariant Identifiers: chr1:g.1956405C>G (hg19) ; chr1:g.2024966C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2024966C>G , CM000663.2:g.2024966C>G	GRCh38
NC_000001.10:g.1956405C>G , CM000663.1:g.1956405C>G	GRCh37
NC_000001.9:g.1946265C>G	NCBI36
NG_008168.1:g.10638C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.93C>G MANE Select	ENSP00000367848.4:p.Tyr31Ter
ENST00000638411.1:c.93C>G	ENSP00000491632.1:p.Tyr31Ter
ENST00000638604.1:n.157C>G
ENST00000638771.1:c.93C>G	ENSP00000492435.1:p.Tyr31Ter
ENST00000639045.1:c.*79C>G	ENSP00000491997.1:n.*79C>G
ENST00000639777.1:n.697C>G
ENST00000639935.1:n.130C>G
ENST00000640030.1:c.33C>G	ENSP00000491411.1:p.Tyr11Ter
ENST00000640067.1:c.93C>G	ENSP00000491844.1:p.Tyr31Ter
ENST00000640423.1:n.102C>G
ENST00000640949.1:c.93C>G	ENSP00000492500.1:p.Tyr31Ter
ENST00000378585.5:c.93C>G	ENSP00000367848.4:p.Tyr31Ter
NM_000815.4:c.93C>G	NP_000806.2:p.Tyr31Ter
XM_011541194.1:c.132C>G	XP_011539496.1:p.Tyr44Ter
XM_011541194.3:c.132C>G	XP_011539496.1:p.Tyr44Ter
XM_017000936.1:c.798C>G	XP_016856425.1:p.Tyr266Ter
NM_000815.5:c.93C>G MANE Select	NP_000806.2:p.Tyr31Ter