Canonical Allele Identifier: CA2293855871

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522156_31522161delinsAATCGT , CM000680.2:g.31522156_31522161delinsAATCGT	GRCh38
NC_000018.9:g.29102119_29102124delinsAATCGT , CM000680.1:g.29102119_29102124delinsAATCGT	GRCh37
NC_000018.8:g.27356117_27356122delinsAATCGT	NCBI36
NG_007072.3:g.28915_28920delinsAATCGT , LRG_397:g.28915_28920delinsAATCGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.428_433delinsAATCGT
ENST00000682241.2:c.597_602delinsAATCGT	ENSP00000507600.2:p.Arg199=
ENST00000683614.2:n.428_433delinsAATCGT
ENST00000682087.1:c.428_433delinsAATCGT
ENST00000682241.1:c.428_433delinsAATCGT
ENST00000683614.1:c.428_433delinsAATCGT
ENST00000683654.1:c.597_602delinsAATCGT	ENSP00000506971.1:p.Arg199=
ENST00000684461.1:n.1267_1272delinsAATCGT
ENST00000261590.13:c.597_602delinsAATCGT MANE Select	ENSP00000261590.8:p.Arg199=
ENST00000261590.12:c.597_602delinsAATCGT	ENSP00000261590.8:p.Arg199=
ENST00000585206.1:c.597_602delinsAATCGT	ENSP00000462503.1:p.Arg199=
NM_001943.3:c.597_602delinsAATCGT , LRG_397t1:c.597_602delinsAATCGT	NP_001934.2:p.Arg199=
NM_001943.4:c.597_602delinsAATCGT	NP_001934.2:p.Arg199=
XM_024451095.1:c.63_68delinsAATCGT	XP_024306863.1:p.Arg21=
NM_001943.5:c.597_602delinsAATCGT MANE Select	NP_001934.2:p.Arg199=