Canonical Allele Identifier: CA1608615474
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7579994G= , CM000668.2:g.7579994G= GRCh38
NC_000006.11:g.7580227G= , CM000668.1:g.7580227G= GRCh37
NC_000006.10:g.7525226G= NCBI36
NG_008803.1:g.43358G= , LRG_423:g.43358G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.3804G= ENSP00000518230.1:p.Arg1268=
ENST00000379802.8:c.3804G= MANE Select ENSP00000369129.3:p.Arg1268=
ENST00000379802.7:c.3804G= ENSP00000369129.3:p.Arg1268=
ENST00000418664.2:c.3582+222G= ENSP00000396591.2:n.3582+222G=
NM_001008844.1:c.3582+222G= NP_001008844.1:n.3582+222G=
NM_004415.2:c.3804G= , LRG_423t1:c.3804G= NP_004406.2:p.Arg1268=
XM_011514323.1:c.3804G= XP_011512625.1:p.Arg1268=
NM_001008844.2:c.3582+222G= NP_001008844.1:n.3582+222G=
NM_001319034.1:c.3804G= NP_001305963.1:p.Arg1268=
NM_004415.3:c.3804G= NP_004406.2:p.Arg1268=
NM_004415.4:c.3804G= MANE Select NP_004406.2:p.Arg1268=
NM_001008844.3:c.3582+222G= NP_001008844.1:n.3582+222G=
NM_001319034.2:c.3804G= NP_001305963.1:p.Arg1268=