Canonical Allele Identifier: CA1608606850
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7582985_7582986delinsGA , CM000668.2:g.7582985_7582986delinsGA GRCh38
NC_000006.11:g.7583218_7583219delinsGA , CM000668.1:g.7583218_7583219delinsGA GRCh37
NC_000006.10:g.7528217_7528218delinsGA NCBI36
NG_008803.1:g.46349_46350delinsGA , LRG_423:g.46349_46350delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.4394_4395delinsGA ENSP00000518230.1:p.Arg1465=
ENST00000379802.8:c.5723_5724delinsGA MANE Select ENSP00000369129.3:p.Arg1908=
ENST00000379802.7:c.5723_5724delinsGA ENSP00000369129.3:p.Arg1908=
ENST00000418664.2:c.3926_3927delinsGA ENSP00000396591.2:p.Arg1309=
NM_001008844.1:c.3926_3927delinsGA NP_001008844.1:p.Arg1309=
NM_004415.2:c.5723_5724delinsGA , LRG_423t1:c.5723_5724delinsGA NP_004406.2:p.Arg1908=
XM_011514323.1:c.4394_4395delinsGA XP_011512625.1:p.Arg1465=
NM_001008844.2:c.3926_3927delinsGA NP_001008844.1:p.Arg1309=
NM_001319034.1:c.4394_4395delinsGA NP_001305963.1:p.Arg1465=
NM_004415.3:c.5723_5724delinsGA NP_004406.2:p.Arg1908=
NM_004415.4:c.5723_5724delinsGA MANE Select NP_004406.2:p.Arg1908=
NM_001008844.3:c.3926_3927delinsGA NP_001008844.1:p.Arg1309=
NM_001319034.2:c.4394_4395delinsGA NP_001305963.1:p.Arg1465=