Canonical Allele Identifier: CA402146802
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546190C>A , CM000680.2:g.31546190C>A GRCh38
NC_000018.9:g.29126153C>A , CM000680.1:g.29126153C>A GRCh37
NC_000018.8:g.27380151C>A NCBI36
NG_007072.3:g.52949C>A , LRG_397:g.52949C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2804C>A (DSG2) MANE Select ENSP00000261590.8:p.Ala935Glu
ENST00000261590.12:c.2804C>A (DSG2) ENSP00000261590.8:p.Ala935Glu
NM_001943.3:c.2804C>A , LRG_397t1:c.2804C>A (DSG2) NP_001934.2:p.Ala935Glu
NR_045216.1:n.1346-284G>T (DSG2-AS1)
NM_001943.4:c.2804C>A (DSG2) NP_001934.2:p.Ala935Glu
XM_024451095.1:c.2270C>A (DSG2) XP_024306863.1:p.Ala757Glu
NM_001943.5:c.2804C>A (DSG2) MANE Select NP_001934.2:p.Ala935Glu