Canonical Allele Identifier: CA2293845631
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498179_31498184delinsGGAGCC , CM000680.2:g.31498179_31498184delinsGGAGCC GRCh38
NC_000018.9:g.29078142_29078147delinsGGAGCC , CM000680.1:g.29078142_29078147delinsGGAGCC GRCh37
NC_000018.8:g.27332140_27332145delinsGGAGCC NCBI36
NG_007072.3:g.4938_4943delinsGGAGCC , LRG_397:g.4938_4943delinsGGAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.-73_-68delinsGGAGCC MANE Select ENSP00000261590.8:n.-73_-68delinsGGAGCC
ENST00000261590.12:c.-73_-68delinsGGAGCC ENSP00000261590.8:n.-73_-68delinsGGAGCC
NM_001943.3:c.-73_-68delinsGGAGCC , LRG_397t1:c.-73_-68delinsGGAGCC NP_001934.2:n.-73_-68delinsGGAGCC
NM_001943.4:c.-73_-68delinsGGAGCC NP_001934.2:n.-73_-68delinsGGAGCC
NM_001943.5:c.-73_-68delinsGGAGCC MANE Select NP_001934.2:n.-73_-68delinsGGAGCC