Canonical Allele Identifier: CA1608615671
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7585755G= , CM000668.2:g.7585755G= GRCh38
NC_000006.11:g.7585988G= , CM000668.1:g.7585988G= GRCh37
NC_000006.10:g.7530987G= NCBI36
NG_008803.1:g.49119G= , LRG_423:g.49119G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.7164G= ENSP00000518230.1:p.Ser2388=
ENST00000379802.8:c.8493G= MANE Select ENSP00000369129.3:p.Ser2831=
ENST00000379802.7:c.8493G= ENSP00000369129.3:p.Ser2831=
ENST00000418664.2:c.6696G= ENSP00000396591.2:p.Ser2232=
NM_001008844.1:c.6696G= NP_001008844.1:p.Ser2232=
NM_004415.2:c.8493G= , LRG_423t1:c.8493G= NP_004406.2:p.Ser2831=
XM_011514323.1:c.7164G= XP_011512625.1:p.Ser2388=
NM_001008844.2:c.6696G= NP_001008844.1:p.Ser2232=
NM_001319034.1:c.7164G= NP_001305963.1:p.Ser2388=
NM_004415.3:c.8493G= NP_004406.2:p.Ser2831=
NM_004415.4:c.8493G= MANE Select NP_004406.2:p.Ser2831=
NM_001008844.3:c.6696G= NP_001008844.1:p.Ser2232=
NM_001319034.2:c.7164G= NP_001305963.1:p.Ser2388=