Canonical Allele Identifier: CA362689172
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1895478
ClinVar RCV Id: RCV002569461
gnomAD v4: 6-7582942-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7582942A>C , CM000668.2:g.7582942A>C GRCh38
NC_000006.11:g.7583175A>C , CM000668.1:g.7583175A>C GRCh37
NC_000006.10:g.7528174A>C NCBI36
NG_008803.1:g.46306A>C , LRG_423:g.46306A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.4351A>C ENSP00000518230.1:p.Ser1451Arg
ENST00000379802.8:c.5680A>C MANE Select ENSP00000369129.3:p.Ser1894Arg
ENST00000379802.7:c.5680A>C ENSP00000369129.3:p.Ser1894Arg
ENST00000418664.2:c.3883A>C ENSP00000396591.2:p.Ser1295Arg
NM_001008844.1:c.3883A>C NP_001008844.1:p.Ser1295Arg
NM_004415.2:c.5680A>C , LRG_423t1:c.5680A>C NP_004406.2:p.Ser1894Arg
XM_011514323.1:c.4351A>C XP_011512625.1:p.Ser1451Arg
NM_001008844.2:c.3883A>C NP_001008844.1:p.Ser1295Arg
NM_001319034.1:c.4351A>C NP_001305963.1:p.Ser1451Arg
NM_004415.3:c.5680A>C NP_004406.2:p.Ser1894Arg
NM_004415.4:c.5680A>C MANE Select NP_004406.2:p.Ser1894Arg
NM_001008844.3:c.3883A>C NP_001008844.1:p.Ser1295Arg
NM_001319034.2:c.4351A>C NP_001305963.1:p.Ser1451Arg