Canonical Allele Identifier: CA1608615856
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7585779C= , CM000668.2:g.7585779C= GRCh38
NC_000006.11:g.7586012C= , CM000668.1:g.7586012C= GRCh37
NC_000006.10:g.7531011C= NCBI36
NG_008803.1:g.49143C= , LRG_423:g.49143C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.7188C= ENSP00000518230.1:p.Ser2396=
ENST00000379802.8:c.8517C= MANE Select ENSP00000369129.3:p.Ser2839=
ENST00000379802.7:c.8517C= ENSP00000369129.3:p.Ser2839=
ENST00000418664.2:c.6720C= ENSP00000396591.2:p.Ser2240=
NM_001008844.1:c.6720C= NP_001008844.1:p.Ser2240=
NM_004415.2:c.8517C= , LRG_423t1:c.8517C= NP_004406.2:p.Ser2839=
XM_011514323.1:c.7188C= XP_011512625.1:p.Ser2396=
NM_001008844.2:c.6720C= NP_001008844.1:p.Ser2240=
NM_001319034.1:c.7188C= NP_001305963.1:p.Ser2396=
NM_004415.3:c.8517C= NP_004406.2:p.Ser2839=
NM_004415.4:c.8517C= MANE Select NP_004406.2:p.Ser2839=
NM_001008844.3:c.6720C= NP_001008844.1:p.Ser2240=
NM_001319034.2:c.7188C= NP_001305963.1:p.Ser2396=