Canonical Allele Identifier: CA402148248
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546456G>A , CM000680.2:g.31546456G>A GRCh38
NC_000018.9:g.29126419G>A , CM000680.1:g.29126419G>A GRCh37
NC_000018.8:g.27380417G>A NCBI36
NG_007072.3:g.53215G>A , LRG_397:g.53215G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3070G>A (DSG2) MANE Select ENSP00000261590.8:p.Ala1024Thr
ENST00000261590.12:c.3070G>A (DSG2) ENSP00000261590.8:p.Ala1024Thr
NM_001943.3:c.3070G>A , LRG_397t1:c.3070G>A (DSG2) NP_001934.2:p.Ala1024Thr
NR_045216.1:n.1346-550C>T (DSG2-AS1)
NM_001943.4:c.3070G>A (DSG2) NP_001934.2:p.Ala1024Thr
XM_024451095.1:c.2536G>A (DSG2) XP_024306863.1:p.Ala846Thr
NM_001943.5:c.3070G>A (DSG2) MANE Select NP_001934.2:p.Ala1024Thr