Canonical Allele Identifier: CA402141436
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542589G>C , CM000680.2:g.31542589G>C GRCh38
NC_000018.9:g.29122552G>C , CM000680.1:g.29122552G>C GRCh37
NC_000018.8:g.27376550G>C NCBI36
NG_007072.3:g.49348G>C , LRG_397:g.49348G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.2071G>C (DSG2) MANE Select ENSP00000261590.8:p.Ala691Pro
ENST00000261590.12:c.2071G>C (DSG2) ENSP00000261590.8:p.Ala691Pro
NM_001943.3:c.2071G>C , LRG_397t1:c.2071G>C (DSG2) NP_001934.2:p.Ala691Pro
NR_045216.1:n.1811-268C>G (DSG2-AS1)
NM_001943.4:c.2071G>C (DSG2) NP_001934.2:p.Ala691Pro
XM_024451095.1:c.1537G>C (DSG2) XP_024306863.1:p.Ala513Pro
NM_001943.5:c.2071G>C (DSG2) MANE Select NP_001934.2:p.Ala691Pro