Canonical Allele Identifier: CA2641412549
Gene: DSG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31519743C>A , CM000680.2:g.31519743C>A GRCh38
NC_000018.9:g.29099706C>A , CM000680.1:g.29099706C>A GRCh37
NC_000018.8:g.27353704C>A NCBI36
NG_007072.3:g.26502C>A , LRG_397:g.26502C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682241.2:c.82-60C>A ENSP00000507600.2:n.82-60C>A
ENST00000683654.1:c.82-60C>A ENSP00000506971.1:n.82-60C>A
ENST00000261590.13:c.82-60C>A MANE Select ENSP00000261590.8:n.82-60C>A
ENST00000261590.12:c.82-60C>A ENSP00000261590.8:n.82-60C>A
ENST00000585206.1:c.82-60C>A ENSP00000462503.1:n.82-60C>A
NM_001943.3:c.82-60C>A , LRG_397t1:c.82-60C>A NP_001934.2:n.82-60C>A
NM_001943.4:c.82-60C>A NP_001934.2:n.82-60C>A
XM_024451095.1:c.-453-60C>A XP_024306863.1:n.-453-60C>A
NM_001943.5:c.82-60C>A MANE Select NP_001934.2:n.82-60C>A