Canonical Allele Identifier: CA2293854942
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31519799A= , CM000680.2:g.31519799A= GRCh38
NC_000018.9:g.29099762A= , CM000680.1:g.29099762A= GRCh37
NC_000018.8:g.27353760A= NCBI36
NG_007072.3:g.26558A= , LRG_397:g.26558A=

Transcript Alleles

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