Canonical Allele Identifier: CA1608607761
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7583305G= , CM000668.2:g.7583305G= GRCh38
NC_000006.11:g.7583538G= , CM000668.1:g.7583538G= GRCh37
NC_000006.10:g.7528537G= NCBI36
NG_008803.1:g.46669G= , LRG_423:g.46669G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.4714G= ENSP00000518230.1:p.Ala1572=
ENST00000379802.8:c.6043G= MANE Select ENSP00000369129.3:p.Ala2015=
ENST00000379802.7:c.6043G= ENSP00000369129.3:p.Ala2015=
ENST00000418664.2:c.4246G= ENSP00000396591.2:p.Ala1416=
NM_001008844.1:c.4246G= NP_001008844.1:p.Ala1416=
NM_004415.2:c.6043G= , LRG_423t1:c.6043G= NP_004406.2:p.Ala2015=
XM_011514323.1:c.4714G= XP_011512625.1:p.Ala1572=
NM_001008844.2:c.4246G= NP_001008844.1:p.Ala1416=
NM_001319034.1:c.4714G= NP_001305963.1:p.Ala1572=
NM_004415.3:c.6043G= NP_004406.2:p.Ala2015=
NM_004415.4:c.6043G= MANE Select NP_004406.2:p.Ala2015=
NM_001008844.3:c.4246G= NP_001008844.1:p.Ala1416=
NM_001319034.2:c.4714G= NP_001305963.1:p.Ala1572=