Canonical Allele Identifier: CA503767193

Gene: DSG2 DSG2-AS1

Linked Data

• MyVariant Identifiers: chr18:g.29126661C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31546698C>G , CM000680.2:g.31546698C>G	GRCh38
NC_000018.9:g.29126661C>G , CM000680.1:g.29126661C>G	GRCh37
NC_000018.8:g.27380659C>G	NCBI36
NG_007072.3:g.53457C>G , LRG_397:g.53457C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261590.13:c.3312C>G (DSG2) MANE Select	ENSP00000261590.8:p.Ser1104=
ENST00000261590.12:c.3312C>G (DSG2)	ENSP00000261590.8:p.Ser1104=
NM_001943.3:c.3312C>G , LRG_397t1:c.3312C>G (DSG2)	NP_001934.2:p.Ser1104=
NR_045216.1:n.1346-792G>C (DSG2-AS1)
NM_001943.4:c.3312C>G (DSG2)	NP_001934.2:p.Ser1104=
XM_024451095.1:c.2778C>G (DSG2)	XP_024306863.1:p.Ser926=
NM_001943.5:c.3312C>G (DSG2) MANE Select	NP_001934.2:p.Ser1104=