Canonical Allele Identifier: CA1608613510
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7579315_7579317delinsGAC , CM000668.2:g.7579315_7579317delinsGAC GRCh38
NC_000006.11:g.7579548_7579550delinsGAC , CM000668.1:g.7579548_7579550delinsGAC GRCh37
NC_000006.10:g.7524547_7524549delinsGAC NCBI36
NG_008803.1:g.42679_42681delinsGAC , LRG_423:g.42679_42681delinsGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.3125_3127delinsGAC ENSP00000518230.1:p.Arg1042=
ENST00000379802.8:c.3125_3127delinsGAC MANE Select ENSP00000369129.3:p.Arg1042=
ENST00000379802.7:c.3125_3127delinsGAC ENSP00000369129.3:p.Arg1042=
ENST00000418664.2:c.3125_3127delinsGAC ENSP00000396591.2:p.Arg1042=
NM_001008844.1:c.3125_3127delinsGAC NP_001008844.1:p.Arg1042=
NM_004415.2:c.3125_3127delinsGAC , LRG_423t1:c.3125_3127delinsGAC NP_004406.2:p.Arg1042=
XM_011514323.1:c.3125_3127delinsGAC XP_011512625.1:p.Arg1042=
NM_001008844.2:c.3125_3127delinsGAC NP_001008844.1:p.Arg1042=
NM_001319034.1:c.3125_3127delinsGAC NP_001305963.1:p.Arg1042=
NM_004415.3:c.3125_3127delinsGAC NP_004406.2:p.Arg1042=
NM_004415.4:c.3125_3127delinsGAC MANE Select NP_004406.2:p.Arg1042=
NM_001008844.3:c.3125_3127delinsGAC NP_001008844.1:p.Arg1042=
NM_001319034.2:c.3125_3127delinsGAC NP_001305963.1:p.Arg1042=