Canonical Allele Identifier: CA2293855479

Gene: DSG2

Linked Data

• dbSNP Id: rs2073125908

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31521183_31521184insTAAAT , CM000680.2:g.31521183_31521184insTAAAT	GRCh38
NC_000018.9:g.29101146_29101147insTAAAT , CM000680.1:g.29101146_29101147insTAAAT	GRCh37
NC_000018.8:g.27355144_27355145insTAAAT	NCBI36
NG_007072.3:g.27942_27943insTAAAT , LRG_397:g.27942_27943insTAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.294_295insTAAAT
ENST00000682241.2:c.463_464insTAAAT	ENSP00000507600.2:p.Asn155IlefsTer19
ENST00000683614.2:n.294_295insTAAAT
ENST00000682087.1:c.294_295insTAAAT
ENST00000682241.1:c.294_295insTAAAT
ENST00000683614.1:c.294_295insTAAAT
ENST00000683654.1:c.463_464insTAAAT	ENSP00000506971.1:p.Asn155IlefsTer19
ENST00000684461.1:n.294_295insTAAAT
ENST00000261590.13:c.463_464insTAAAT MANE Select	ENSP00000261590.8:p.Asn155IlefsTer19
ENST00000261590.12:c.463_464insTAAAT	ENSP00000261590.8:p.Asn155IlefsTer19
ENST00000585206.1:c.463_464insTAAAT	ENSP00000462503.1:p.Asn155IlefsTer19
NM_001943.3:c.463_464insTAAAT , LRG_397t1:c.463_464insTAAAT	NP_001934.2:p.Asn155IlefsTer19
NM_001943.4:c.463_464insTAAAT	NP_001934.2:p.Asn155IlefsTer19
XM_024451095.1:c.-72_-71insTAAAT	XP_024306863.1:n.-72_-71insTAAAT
NM_001943.5:c.463_464insTAAAT MANE Select	NP_001934.2:p.Asn155IlefsTer19