Canonical Allele Identifier: CA004201
Gene: DSP HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.7581105G>A
GRCh37 chr6:g.7581338G>A
Revel Score:
ENST00000379802 (MANE Select) 0.192
gnomAD v2:
6:7581338 G / A
gnomAD v3:
6:7581105 G / A
gnomAD v4:
chr6-7581105-G-A
Joint Max Group AF 0.00004345 (EAS)
Genomes Max Group AF 0.00001972 (NFE)
Exomes Max Group AF 0.00004907 (EAS)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7581105G>A , CM000668.2:g.7581105G>A GRCh38
NC_000006.11:g.7581338G>A , CM000668.1:g.7581338G>A GRCh37
NC_000006.10:g.7526337G>A NCBI36
NG_008803.1:g.44469G>A , LRG_423:g.44469G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.4050+865G>A ENSP00000518230.1:n.4050+865G>A
ENST00000379802.8:c.4915G>A MANE Select ENSP00000369129.3:p.Val1639Met
ENST00000379802.7:c.4915G>A ENSP00000369129.3:p.Val1639Met
ENST00000418664.2:c.3582+1333G>A ENSP00000396591.2:n.3582+1333G>A
NM_001008844.1:c.3582+1333G>A NP_001008844.1:n.3582+1333G>A
NM_004415.2:c.4915G>A , LRG_423t1:c.4915G>A NP_004406.2:p.Val1639Met
XM_011514323.1:c.4050+865G>A XP_011512625.1:n.4050+865G>A
NM_001008844.2:c.3582+1333G>A NP_001008844.1:n.3582+1333G>A
NM_001319034.1:c.4050+865G>A NP_001305963.1:n.4050+865G>A
NM_004415.3:c.4915G>A NP_004406.2:p.Val1639Met
NM_004415.4:c.4915G>A MANE Select NP_004406.2:p.Val1639Met
NM_001008844.3:c.3582+1333G>A NP_001008844.1:n.3582+1333G>A
NM_001319034.2:c.4050+865G>A NP_001305963.1:n.4050+865G>A
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