Canonical Allele Identifier: CA2293866549
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2073319660

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547255_31547270del , CM000680.2:g.31547255_31547270del GRCh38
NC_000018.9:g.29127218_29127233del , CM000680.1:g.29127218_29127233del GRCh37
NC_000018.8:g.27381216_27381231del NCBI36
NG_007072.3:g.54014_54029del , LRG_397:g.54014_54029del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*512_*527del (DSG2) MANE Select ENSP00000261590.8:n.*512_*527del
ENST00000261590.12:c.*512_*527del (DSG2) ENSP00000261590.8:n.*512_*527del
NM_001943.3:c.*512_*527del , LRG_397t1:c.*512_*527del (DSG2) NP_001934.2:n.*512_*527del
NR_045216.1:n.1346-1360_1346-1345del (DSG2-AS1)
NM_001943.4:c.*512_*527del (DSG2) NP_001934.2:n.*512_*527del
XM_024451095.1:c.*512_*527del (DSG2) XP_024306863.1:n.*512_*527del
NM_001943.5:c.*512_*527del (DSG2) MANE Select NP_001934.2:n.*512_*527del