Canonical Allele Identifier: CA337955727

Gene: GABRD

Linked Data

• COSMIC: COSM335537
• MyVariant Identifiers: chr1:g.1956476T>C (hg19) ; chr1:g.2025037T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2025037T>C , CM000663.2:g.2025037T>C	GRCh38
NC_000001.10:g.1956476T>C , CM000663.1:g.1956476T>C	GRCh37
NC_000001.9:g.1946336T>C	NCBI36
NG_008168.1:g.10709T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.164T>C MANE Select	ENSP00000367848.4:p.Phe55Ser
ENST00000638411.1:c.164T>C	ENSP00000491632.1:p.Phe55Ser
ENST00000638604.1:n.228T>C
ENST00000638771.1:c.164T>C	ENSP00000492435.1:p.Phe55Ser
ENST00000639045.1:c.*150T>C	ENSP00000491997.1:n.*150T>C
ENST00000639777.1:n.768T>C
ENST00000639935.1:n.201T>C
ENST00000640030.1:c.104T>C	ENSP00000491411.1:p.Phe35Ser
ENST00000640067.1:c.164T>C	ENSP00000491844.1:p.Phe55Ser
ENST00000640423.1:n.173T>C
ENST00000640949.1:c.164T>C	ENSP00000492500.1:p.Phe55Ser
ENST00000378585.5:c.164T>C	ENSP00000367848.4:p.Phe55Ser
NM_000815.4:c.164T>C	NP_000806.2:p.Phe55Ser
XM_011541194.1:c.203T>C	XP_011539496.1:p.Phe68Ser
XM_011541194.3:c.203T>C	XP_011539496.1:p.Phe68Ser
XM_017000936.1:c.869T>C	XP_016856425.1:p.Phe290Ser
NM_000815.5:c.164T>C MANE Select	NP_000806.2:p.Phe55Ser