Canonical Allele Identifier: CA2966933680
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31522025dup , CM000680.2:g.31522025dup GRCh38
NC_000018.9:g.29101988dup , CM000680.1:g.29101988dup GRCh37
NC_000018.8:g.27355986dup NCBI36
NG_007072.3:g.28784dup , LRG_397:g.28784dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682087.2:n.355-58dup
ENST00000682241.2:c.524-58dup ENSP00000507600.2:n.524-58dup
ENST00000683614.2:n.355-58dup
ENST00000682087.1:c.355-58dup
ENST00000682241.1:c.355-58dup
ENST00000683614.1:c.355-58dup
ENST00000683654.1:c.524-58dup ENSP00000506971.1:n.524-58dup
ENST00000684461.1:n.1136dup
ENST00000261590.13:c.524-58dup MANE Select ENSP00000261590.8:n.524-58dup
ENST00000261590.12:c.524-58dup ENSP00000261590.8:n.524-58dup
ENST00000585206.1:c.524-58dup ENSP00000462503.1:n.524-58dup
NM_001943.3:c.524-58dup , LRG_397t1:c.524-58dup NP_001934.2:n.524-58dup
NM_001943.4:c.524-58dup NP_001934.2:n.524-58dup
XM_024451095.1:c.-11-58dup XP_024306863.1:n.-11-58dup
NM_001943.5:c.524-58dup MANE Select NP_001934.2:n.524-58dup