Canonical Allele Identifier: CA041256
Gene: DSG2 HGNC NCBI
COSMIC:
COSM987622
MyVariant.info:
GRCh38 chr18:g.31531017G>A
GRCh37 chr18:g.29110980G>A
Revel Score:
ENST00000261590 (MANE Select) 0.024
gnomAD v2:
18:29110980 G / A
gnomAD v4:
chr18-31531017-G-A
Joint Max Group AF 0.00000442 (AFR)
Exomes Max Group AF 0.00000989 (AFR)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531017G>A , CM000680.2:g.31531017G>A GRCh38
NC_000018.9:g.29110980G>A , CM000680.1:g.29110980G>A GRCh37
NC_000018.8:g.27364978G>A NCBI36
NG_007072.3:g.37776G>A , LRG_397:g.37776G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000683614.2:n.876G>A
ENST00000683614.1:c.876G>A
ENST00000261590.13:c.1045G>A MANE Select ENSP00000261590.8:p.Asp349Asn
ENST00000261590.12:c.1045G>A ENSP00000261590.8:p.Asp349Asn
NM_001943.3:c.1045G>A , LRG_397t1:c.1045G>A NP_001934.2:p.Asp349Asn
NM_001943.4:c.1045G>A NP_001934.2:p.Asp349Asn
XM_024451095.1:c.511G>A XP_024306863.1:p.Asp171Asn
NM_001943.5:c.1045G>A MANE Select NP_001934.2:p.Asp349Asn
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