Canonical Allele Identifier: CA337955777

Gene: GABRD

Linked Data

• MyVariant Identifiers: chr1:g.1956488T>A (hg19) ; chr1:g.2025049T>A (hg38)
• PubMed: PMID:28263302

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2025049T>A , CM000663.2:g.2025049T>A	GRCh38
NC_000001.10:g.1956488T>A , CM000663.1:g.1956488T>A	GRCh37
NC_000001.9:g.1946348T>A	NCBI36
NG_008168.1:g.10721T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.176T>A MANE Select	ENSP00000367848.4:p.Ile59Asn
ENST00000638411.1:c.176T>A	ENSP00000491632.1:p.Ile59Asn
ENST00000638604.1:n.240T>A
ENST00000638771.1:c.176T>A	ENSP00000492435.1:p.Ile59Asn
ENST00000639045.1:c.*162T>A	ENSP00000491997.1:n.*162T>A
ENST00000639777.1:n.780T>A
ENST00000639935.1:n.213T>A
ENST00000640030.1:c.116T>A	ENSP00000491411.1:p.Ile39Asn
ENST00000640067.1:c.176T>A	ENSP00000491844.1:p.Ile59Asn
ENST00000640423.1:n.185T>A
ENST00000640949.1:c.176T>A	ENSP00000492500.1:p.Ile59Asn
ENST00000378585.5:c.176T>A	ENSP00000367848.4:p.Ile59Asn
NM_000815.4:c.176T>A	NP_000806.2:p.Ile59Asn
XM_011541194.1:c.215T>A	XP_011539496.1:p.Ile72Asn
XM_011541194.3:c.215T>A	XP_011539496.1:p.Ile72Asn
XM_017000936.1:c.881T>A	XP_016856425.1:p.Ile294Asn
NM_000815.5:c.176T>A MANE Select	NP_000806.2:p.Ile59Asn