Canonical Allele Identifier: CA629453691
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1391168117

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31545694_31545704del , CM000680.2:g.31545694_31545704del GRCh38
NC_000018.9:g.29125657_29125667del , CM000680.1:g.29125657_29125667del GRCh37
NC_000018.8:g.27379655_27379665del NCBI36
NG_007072.3:g.52453_52463del , LRG_397:g.52453_52463del

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.2335-27_2335-17del (DSG2) MANE Select ENSP00000261590.8:n.2335-27_2335-17del
ENST00000261590.12:c.2335-27_2335-17del (DSG2) ENSP00000261590.8:n.2335-27_2335-17del
NM_001943.3:c.2335-27_2335-17del , LRG_397t1:c.2335-27_2335-17del (DSG2) NP_001934.2:n.2335-27_2335-17del
NR_045216.1:n.1516+40_1516+50del (DSG2-AS1)
NM_001943.4:c.2335-27_2335-17del (DSG2) NP_001934.2:n.2335-27_2335-17del
XM_024451095.1:c.1801-27_1801-17del (DSG2) XP_024306863.1:n.1801-27_1801-17del
NM_001943.5:c.2335-27_2335-17del (DSG2) MANE Select NP_001934.2:n.2335-27_2335-17del