Canonical Allele Identifier: CA362676339
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3069634
ClinVar RCV Id: RCV004008178
gnomAD v4: 6-7568464-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7568464A>G , CM000668.2:g.7568464A>G GRCh38
NC_000006.11:g.7568697A>G , CM000668.1:g.7568697A>G GRCh37
NC_000006.10:g.7513696A>G NCBI36
NG_008803.1:g.31828A>G , LRG_423:g.31828A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.1294A>G ENSP00000518230.1:p.Lys432Glu
ENST00000682228.1:n.1479A>G
ENST00000379802.8:c.1294A>G MANE Select ENSP00000369129.3:p.Lys432Glu
ENST00000379802.7:c.1294A>G ENSP00000369129.3:p.Lys432Glu
ENST00000418664.2:c.1294A>G ENSP00000396591.2:p.Lys432Glu
NM_001008844.1:c.1294A>G NP_001008844.1:p.Lys432Glu
NM_004415.2:c.1294A>G , LRG_423t1:c.1294A>G NP_004406.2:p.Lys432Glu
XM_011514323.1:c.1294A>G XP_011512625.1:p.Lys432Glu
NM_001008844.2:c.1294A>G NP_001008844.1:p.Lys432Glu
NM_001319034.1:c.1294A>G NP_001305963.1:p.Lys432Glu
NM_004415.3:c.1294A>G NP_004406.2:p.Lys432Glu
NM_004415.4:c.1294A>G MANE Select NP_004406.2:p.Lys432Glu
NM_001008844.3:c.1294A>G NP_001008844.1:p.Lys432Glu
NM_001319034.2:c.1294A>G NP_001305963.1:p.Lys432Glu