Canonical Allele Identifier: CA1608613473
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7585162A= , CM000668.2:g.7585162A= GRCh38
NC_000006.11:g.7585395A= , CM000668.1:g.7585395A= GRCh37
NC_000006.10:g.7530394A= NCBI36
NG_008803.1:g.48526A= , LRG_423:g.48526A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.6571A= ENSP00000518230.1:p.Thr2191=
ENST00000379802.8:c.7900A= MANE Select ENSP00000369129.3:p.Thr2634=
ENST00000379802.7:c.7900A= ENSP00000369129.3:p.Thr2634=
ENST00000418664.2:c.6103A= ENSP00000396591.2:p.Thr2035=
NM_001008844.1:c.6103A= NP_001008844.1:p.Thr2035=
NM_004415.2:c.7900A= , LRG_423t1:c.7900A= NP_004406.2:p.Thr2634=
XM_011514323.1:c.6571A= XP_011512625.1:p.Thr2191=
NM_001008844.2:c.6103A= NP_001008844.1:p.Thr2035=
NM_001319034.1:c.6571A= NP_001305963.1:p.Thr2191=
NM_004415.3:c.7900A= NP_004406.2:p.Thr2634=
NM_004415.4:c.7900A= MANE Select NP_004406.2:p.Thr2634=
NM_001008844.3:c.6103A= NP_001008844.1:p.Thr2035=
NM_001319034.2:c.6571A= NP_001305963.1:p.Thr2191=