Canonical Allele Identifier: CA047791
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 919290
ClinVar RCV Id: RCV001177389
dbSNP Id: rs539821357

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546425C>T , CM000680.2:g.31546425C>T GRCh38
NC_000018.9:g.29126388C>T , CM000680.1:g.29126388C>T GRCh37
NC_000018.8:g.27380386C>T NCBI36
NG_007072.3:g.53184C>T , LRG_397:g.53184C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.3039C>T (DSG2) MANE Select ENSP00000261590.8:p.Tyr1013=
ENST00000261590.12:c.3039C>T (DSG2) ENSP00000261590.8:p.Tyr1013=
NM_001943.3:c.3039C>T , LRG_397t1:c.3039C>T (DSG2) NP_001934.2:p.Tyr1013=
NR_045216.1:n.1346-519G>A (DSG2-AS1)
NM_001943.4:c.3039C>T (DSG2) NP_001934.2:p.Tyr1013=
XM_024451095.1:c.2505C>T (DSG2) XP_024306863.1:p.Tyr835=
NM_001943.5:c.3039C>T (DSG2) MANE Select NP_001934.2:p.Tyr1013=