Canonical Allele Identifier: CA362689499
Gene: DSP HGNC NCBI

Linked Data

dbSNP Id: rs1759499845
gnomAD v3: 6-7583090-G-A
gnomAD v4: 6-7583090-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7583090G>A , CM000668.2:g.7583090G>A GRCh38
NC_000006.11:g.7583323G>A , CM000668.1:g.7583323G>A GRCh37
NC_000006.10:g.7528322G>A NCBI36
NG_008803.1:g.46454G>A , LRG_423:g.46454G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.4499G>A ENSP00000518230.1:p.Arg1500Lys
ENST00000379802.8:c.5828G>A MANE Select ENSP00000369129.3:p.Arg1943Lys
ENST00000379802.7:c.5828G>A ENSP00000369129.3:p.Arg1943Lys
ENST00000418664.2:c.4031G>A ENSP00000396591.2:p.Arg1344Lys
NM_001008844.1:c.4031G>A NP_001008844.1:p.Arg1344Lys
NM_004415.2:c.5828G>A , LRG_423t1:c.5828G>A NP_004406.2:p.Arg1943Lys
XM_011514323.1:c.4499G>A XP_011512625.1:p.Arg1500Lys
NM_001008844.2:c.4031G>A NP_001008844.1:p.Arg1344Lys
NM_001319034.1:c.4499G>A NP_001305963.1:p.Arg1500Lys
NM_004415.3:c.5828G>A NP_004406.2:p.Arg1943Lys
NM_004415.4:c.5828G>A MANE Select NP_004406.2:p.Arg1943Lys
NM_001008844.3:c.4031G>A NP_001008844.1:p.Arg1344Lys
NM_001319034.2:c.4499G>A NP_001305963.1:p.Arg1500Lys