Canonical Allele Identifier: CA2293855926

Gene: DSG2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31522282_31522284delinsACT , CM000680.2:g.31522282_31522284delinsACT	GRCh38
NC_000018.9:g.29102245_29102247delinsACT , CM000680.1:g.29102245_29102247delinsACT	GRCh37
NC_000018.8:g.27356243_27356245delinsACT	NCBI36
NG_007072.3:g.29041_29043delinsACT , LRG_397:g.29041_29043delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.521+33_521+35delinsACT
ENST00000682241.2:c.690+33_690+35delinsACT	ENSP00000507600.2:n.690+33_690+35delinsACT
ENST00000683614.2:n.521+33_521+35delinsACT
ENST00000682087.1:c.521+33_521+35delinsACT
ENST00000682241.1:c.521+33_521+35delinsACT
ENST00000683614.1:c.521+33_521+35delinsACT
ENST00000683654.1:c.690+33_690+35delinsACT	ENSP00000506971.1:n.690+33_690+35delinsACT
ENST00000684461.1:n.1393_1395delinsACT
ENST00000261590.13:c.690+33_690+35delinsACT MANE Select	ENSP00000261590.8:n.690+33_690+35delinsACT
ENST00000261590.12:c.690+33_690+35delinsACT	ENSP00000261590.8:n.690+33_690+35delinsACT
ENST00000585206.1:c.*24_*26delinsACT	ENSP00000462503.1:n.*24_*26delinsACT
NM_001943.3:c.690+33_690+35delinsACT , LRG_397t1:c.690+33_690+35delinsACT	NP_001934.2:n.690+33_690+35delinsACT
NM_001943.4:c.690+33_690+35delinsACT	NP_001934.2:n.690+33_690+35delinsACT
XM_024451095.1:c.156+33_156+35delinsACT	XP_024306863.1:n.156+33_156+35delinsACT
NM_001943.5:c.690+33_690+35delinsACT MANE Select	NP_001934.2:n.690+33_690+35delinsACT