Canonical Allele Identifier: CA2574176687
Gene: GABRD HGNC NCBI

Linked Data

gnomAD v4: 1-2025107-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2025107C>T , CM000663.2:g.2025107C>T GRCh38
NC_000001.10:g.1956546C>T , CM000663.1:g.1956546C>T GRCh37
NC_000001.9:g.1946406C>T NCBI36
NG_008168.1:g.10779C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378585.7:c.181+53C>T MANE Select ENSP00000367848.4:n.181+53C>T
ENST00000638411.1:c.181+53C>T ENSP00000491632.1:n.181+53C>T
ENST00000638604.1:n.245+53C>T
ENST00000638771.1:c.181+53C>T ENSP00000492435.1:n.181+53C>T
ENST00000639045.1:c.*167+53C>T ENSP00000491997.1:n.*167+53C>T
ENST00000639777.1:n.785+53C>T
ENST00000639935.1:n.218+53C>T
ENST00000640030.1:c.121+53C>T ENSP00000491411.1:n.121+53C>T
ENST00000640067.1:c.181+53C>T ENSP00000491844.1:n.181+53C>T
ENST00000640423.1:n.190+53C>T
ENST00000640949.1:c.181+53C>T ENSP00000492500.1:n.181+53C>T
ENST00000378585.5:c.181+53C>T ENSP00000367848.4:n.181+53C>T
NM_000815.4:c.181+53C>T NP_000806.2:n.181+53C>T
XM_011541194.1:c.220+53C>T XP_011539496.1:n.220+53C>T
XM_011541194.3:c.220+53C>T XP_011539496.1:n.220+53C>T
XM_017000936.1:c.886+53C>T XP_016856425.1:n.886+53C>T
NM_000815.5:c.181+53C>T MANE Select NP_000806.2:n.181+53C>T