Canonical Allele Identifier: CA503765966

Gene: DSG2 DSG2-AS1

Linked Data

• MyVariant Identifiers: chr18:g.29122665A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31542702A>G , CM000680.2:g.31542702A>G	GRCh38
NC_000018.9:g.29122665A>G , CM000680.1:g.29122665A>G	GRCh37
NC_000018.8:g.27376663A>G	NCBI36
NG_007072.3:g.49461A>G , LRG_397:g.49461A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261590.13:c.2184A>G (DSG2) MANE Select	ENSP00000261590.8:p.Arg728=
ENST00000261590.12:c.2184A>G (DSG2)	ENSP00000261590.8:p.Arg728=
NM_001943.3:c.2184A>G , LRG_397t1:c.2184A>G (DSG2)	NP_001934.2:p.Arg728=
NR_045216.1:n.1811-381T>C (DSG2-AS1)
NM_001943.4:c.2184A>G (DSG2)	NP_001934.2:p.Arg728=
XM_024451095.1:c.1650A>G (DSG2)	XP_024306863.1:p.Arg550=
NM_001943.5:c.2184A>G (DSG2) MANE Select	NP_001934.2:p.Arg728=