Canonical Allele Identifier: CA503766513
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29126307G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546344G>A , CM000680.2:g.31546344G>A GRCh38
NC_000018.9:g.29126307G>A , CM000680.1:g.29126307G>A GRCh37
NC_000018.8:g.27380305G>A NCBI36
NG_007072.3:g.53103G>A , LRG_397:g.53103G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.2958G>A (DSG2) MANE Select ENSP00000261590.8:p.Val986=
ENST00000261590.12:c.2958G>A (DSG2) ENSP00000261590.8:p.Val986=
NM_001943.3:c.2958G>A , LRG_397t1:c.2958G>A (DSG2) NP_001934.2:p.Val986=
NR_045216.1:n.1346-438C>T (DSG2-AS1)
NM_001943.4:c.2958G>A (DSG2) NP_001934.2:p.Val986=
XM_024451095.1:c.2424G>A (DSG2) XP_024306863.1:p.Val808=
NM_001943.5:c.2958G>A (DSG2) MANE Select NP_001934.2:p.Val986=