Canonical Allele Identifier: CA2560997464
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31519784C>T , CM000680.2:g.31519784C>T GRCh38
NC_000018.9:g.29099747C>T , CM000680.1:g.29099747C>T GRCh37
NC_000018.8:g.27353745C>T NCBI36
NG_007072.3:g.26543C>T , LRG_397:g.26543C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682241.2:c.82-19C>T ENSP00000507600.2:n.82-19C>T
ENST00000683654.1:c.82-19C>T ENSP00000506971.1:n.82-19C>T
ENST00000261590.13:c.82-19C>T MANE Select ENSP00000261590.8:n.82-19C>T
ENST00000261590.12:c.82-19C>T ENSP00000261590.8:n.82-19C>T
ENST00000585206.1:c.82-19C>T ENSP00000462503.1:n.82-19C>T
NM_001943.3:c.82-19C>T , LRG_397t1:c.82-19C>T NP_001934.2:n.82-19C>T
NM_001943.4:c.82-19C>T NP_001934.2:n.82-19C>T
XM_024451095.1:c.-453-19C>T XP_024306863.1:n.-453-19C>T
NM_001943.5:c.82-19C>T MANE Select NP_001934.2:n.82-19C>T