Canonical Allele Identifier: CA2293866107
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546276_31546277delinsAC , CM000680.2:g.31546276_31546277delinsAC GRCh38
NC_000018.9:g.29126239_29126240delinsAC , CM000680.1:g.29126239_29126240delinsAC GRCh37
NC_000018.8:g.27380237_27380238delinsAC NCBI36
NG_007072.3:g.53035_53036delinsAC , LRG_397:g.53035_53036delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2890_2891delinsAC (DSG2) MANE Select ENSP00000261590.8:p.Thr964=
ENST00000261590.12:c.2890_2891delinsAC (DSG2) ENSP00000261590.8:p.Thr964=
NM_001943.3:c.2890_2891delinsAC , LRG_397t1:c.2890_2891delinsAC (DSG2) NP_001934.2:p.Thr964=
NR_045216.1:n.1346-371_1346-370delinsGT (DSG2-AS1)
NM_001943.4:c.2890_2891delinsAC (DSG2) NP_001934.2:p.Thr964=
XM_024451095.1:c.2356_2357delinsAC (DSG2) XP_024306863.1:p.Thr786=
NM_001943.5:c.2890_2891delinsAC (DSG2) MANE Select NP_001934.2:p.Thr964=