Canonical Allele Identifier: CA402134199

Gene: DSG2

Linked Data

• MyVariant Identifiers: chr18:g.29102216A>G (hg19) ; chr18:g.31522253A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522253A>G , CM000680.2:g.31522253A>G	GRCh38
NC_000018.9:g.29102216A>G , CM000680.1:g.29102216A>G	GRCh37
NC_000018.8:g.27356214A>G	NCBI36
NG_007072.3:g.29012A>G , LRG_397:g.29012A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.521+4A>G
ENST00000682241.2:c.690+4A>G	ENSP00000507600.2:n.690+4A>G
ENST00000683614.2:n.521+4A>G
ENST00000682087.1:c.521+4A>G
ENST00000682241.1:c.521+4A>G
ENST00000683614.1:c.521+4A>G
ENST00000683654.1:c.690+4A>G	ENSP00000506971.1:n.690+4A>G
ENST00000684461.1:n.1364A>G
ENST00000261590.13:c.690+4A>G MANE Select	ENSP00000261590.8:n.690+4A>G
ENST00000261590.12:c.690+4A>G	ENSP00000261590.8:n.690+4A>G
ENST00000585206.1:c.694A>G	ENSP00000462503.1:p.Ser232Gly
NM_001943.3:c.690+4A>G , LRG_397t1:c.690+4A>G	NP_001934.2:n.690+4A>G
NM_001943.4:c.690+4A>G	NP_001934.2:n.690+4A>G
XM_024451095.1:c.156+4A>G	XP_024306863.1:n.156+4A>G
NM_001943.5:c.690+4A>G MANE Select	NP_001934.2:n.690+4A>G