Canonical Allele Identifier: CA2293855866

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522148_31522149delinsTC , CM000680.2:g.31522148_31522149delinsTC	GRCh38
NC_000018.9:g.29102111_29102112delinsTC , CM000680.1:g.29102111_29102112delinsTC	GRCh37
NC_000018.8:g.27356109_27356110delinsTC	NCBI36
NG_007072.3:g.28907_28908delinsTC , LRG_397:g.28907_28908delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.420_421delinsTC
ENST00000682241.2:c.589_590delinsTC	ENSP00000507600.2:p.Ser197=
ENST00000683614.2:n.420_421delinsTC
ENST00000682087.1:c.420_421delinsTC
ENST00000682241.1:c.420_421delinsTC
ENST00000683614.1:c.420_421delinsTC
ENST00000683654.1:c.589_590delinsTC	ENSP00000506971.1:p.Ser197=
ENST00000684461.1:n.1259_1260delinsTC
ENST00000261590.13:c.589_590delinsTC MANE Select	ENSP00000261590.8:p.Ser197=
ENST00000261590.12:c.589_590delinsTC	ENSP00000261590.8:p.Ser197=
ENST00000585206.1:c.589_590delinsTC	ENSP00000462503.1:p.Ser197=
NM_001943.3:c.589_590delinsTC , LRG_397t1:c.589_590delinsTC	NP_001934.2:p.Ser197=
NM_001943.4:c.589_590delinsTC	NP_001934.2:p.Ser197=
XM_024451095.1:c.55_56delinsTC	XP_024306863.1:p.Ser19=
NM_001943.5:c.589_590delinsTC MANE Select	NP_001934.2:p.Ser197=