Canonical Allele Identifier: CA133977890
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2775384
dbSNP Id: rs943247894
gnomAD v3: 6-7585648-G-A
gnomAD v4: 6-7585648-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7585648G>A , CM000668.2:g.7585648G>A GRCh38
NC_000006.11:g.7585881G>A , CM000668.1:g.7585881G>A GRCh37
NC_000006.10:g.7530880G>A NCBI36
NG_008803.1:g.49012G>A , LRG_423:g.49012G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.7057G>A ENSP00000518230.1:p.Asp2353Asn
ENST00000379802.8:c.8386G>A MANE Select ENSP00000369129.3:p.Asp2796Asn
ENST00000379802.7:c.8386G>A ENSP00000369129.3:p.Asp2796Asn
ENST00000418664.2:c.6589G>A ENSP00000396591.2:p.Asp2197Asn
NM_001008844.1:c.6589G>A NP_001008844.1:p.Asp2197Asn
NM_004415.2:c.8386G>A , LRG_423t1:c.8386G>A NP_004406.2:p.Asp2796Asn
XM_011514323.1:c.7057G>A XP_011512625.1:p.Asp2353Asn
NM_001008844.2:c.6589G>A NP_001008844.1:p.Asp2197Asn
NM_001319034.1:c.7057G>A NP_001305963.1:p.Asp2353Asn
NM_004415.3:c.8386G>A NP_004406.2:p.Asp2796Asn
NM_004415.4:c.8386G>A MANE Select NP_004406.2:p.Asp2796Asn
NM_001008844.3:c.6589G>A NP_001008844.1:p.Asp2197Asn
NM_001319034.2:c.7057G>A NP_001305963.1:p.Asp2353Asn