Canonical Allele Identifier: CA2642691047
Gene: GABRD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2025166_2025170del , CM000663.2:g.2025166_2025170del GRCh38
NC_000001.10:g.1956605_1956609del , CM000663.1:g.1956605_1956609del GRCh37
NC_000001.9:g.1946465_1946469del NCBI36
NG_008168.1:g.10838_10842del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378585.7:c.181+112_181+116del MANE Select ENSP00000367848.4:n.181+112_181+116del
ENST00000638411.1:c.181+112_181+116del ENSP00000491632.1:n.181+112_181+116del
ENST00000638604.1:n.245+112_245+116del
ENST00000638771.1:c.181+112_181+116del ENSP00000492435.1:n.181+112_181+116del
ENST00000639045.1:c.*167+112_*167+116del ENSP00000491997.1:n.*167+112_*167+116del
ENST00000639777.1:n.785+112_785+116del
ENST00000639935.1:n.218+112_218+116del
ENST00000640030.1:c.121+112_121+116del ENSP00000491411.1:n.121+112_121+116del
ENST00000640067.1:c.181+112_181+116del ENSP00000491844.1:n.181+112_181+116del
ENST00000640423.1:n.190+112_190+116del
ENST00000640949.1:c.181+112_181+116del ENSP00000492500.1:n.181+112_181+116del
ENST00000378585.5:c.181+112_181+116del ENSP00000367848.4:n.181+112_181+116del
NM_000815.4:c.181+112_181+116del NP_000806.2:n.181+112_181+116del
XM_011541194.1:c.220+112_220+116del XP_011539496.1:n.220+112_220+116del
XM_011541194.3:c.220+112_220+116del XP_011539496.1:n.220+112_220+116del
XM_017000936.1:c.886+112_886+116del XP_016856425.1:n.886+112_886+116del
NM_000815.5:c.181+112_181+116del MANE Select NP_000806.2:n.181+112_181+116del