Canonical Allele Identifier: CA2293859872
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531333_31531334delinsCA , CM000680.2:g.31531333_31531334delinsCA GRCh38
NC_000018.9:g.29111296_29111297delinsCA , CM000680.1:g.29111296_29111297delinsCA GRCh37
NC_000018.8:g.27365294_27365295delinsCA NCBI36
NG_007072.3:g.38092_38093delinsCA , LRG_397:g.38092_38093delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000683614.2:n.1192_1193delinsCA
ENST00000683614.1:c.1192_1193delinsCA
ENST00000261590.13:c.1280+81_1280+82delinsCA MANE Select ENSP00000261590.8:n.1280+81_1280+82delinsCA
ENST00000261590.12:c.1280+81_1280+82delinsCA ENSP00000261590.8:n.1280+81_1280+82delinsCA
NM_001943.3:c.1280+81_1280+82delinsCA , LRG_397t1:c.1280+81_1280+82delinsCA NP_001934.2:n.1280+81_1280+82delinsCA
NM_001943.4:c.1280+81_1280+82delinsCA NP_001934.2:n.1280+81_1280+82delinsCA
XM_024451095.1:c.746+81_746+82delinsCA XP_024306863.1:n.746+81_746+82delinsCA
NM_001943.5:c.1280+81_1280+82delinsCA MANE Select NP_001934.2:n.1280+81_1280+82delinsCA