Canonical Allele Identifier: CA402135241

Gene: DSG2

Linked Data

• MyVariant Identifiers: chr18:g.29104527A>G (hg19) ; chr18:g.31524564A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31524564A>G , CM000680.2:g.31524564A>G	GRCh38
NC_000018.9:g.29104527A>G , CM000680.1:g.29104527A>G	GRCh37
NC_000018.8:g.27358525A>G	NCBI36
NG_007072.3:g.31323A>G , LRG_397:g.31323A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.638A>G
ENST00000683614.2:n.638A>G
ENST00000682087.1:c.638A>G
ENST00000683614.1:c.638A>G
ENST00000261590.13:c.807A>G MANE Select	ENSP00000261590.8:p.Ile269Met
ENST00000261590.12:c.807A>G	ENSP00000261590.8:p.Ile269Met
NM_001943.3:c.807A>G , LRG_397t1:c.807A>G	NP_001934.2:p.Ile269Met
NM_001943.4:c.807A>G	NP_001934.2:p.Ile269Met
XM_024451095.1:c.273A>G	XP_024306863.1:p.Ile91Met
NM_001943.5:c.807A>G MANE Select	NP_001934.2:p.Ile269Met