Canonical Allele Identifier: CA2293866218
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546496_31546497delinsAT , CM000680.2:g.31546496_31546497delinsAT GRCh38
NC_000018.9:g.29126459_29126460delinsAT , CM000680.1:g.29126459_29126460delinsAT GRCh37
NC_000018.8:g.27380457_27380458delinsAT NCBI36
NG_007072.3:g.53255_53256delinsAT , LRG_397:g.53255_53256delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3110_3111delinsAT (DSG2) MANE Select ENSP00000261590.8:p.Asn1037=
ENST00000261590.12:c.3110_3111delinsAT (DSG2) ENSP00000261590.8:p.Asn1037=
NM_001943.3:c.3110_3111delinsAT , LRG_397t1:c.3110_3111delinsAT (DSG2) NP_001934.2:p.Asn1037=
NR_045216.1:n.1346-591_1346-590delinsAT (DSG2-AS1)
NM_001943.4:c.3110_3111delinsAT (DSG2) NP_001934.2:p.Asn1037=
XM_024451095.1:c.2576_2577delinsAT (DSG2) XP_024306863.1:p.Asn859=
NM_001943.5:c.3110_3111delinsAT (DSG2) MANE Select NP_001934.2:p.Asn1037=