Canonical Allele Identifier: CA402135343

Gene: DSG2

Linked Data

• MyVariant Identifiers: chr18:g.31524685_31524686del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31524688_31524689del , CM000680.2:g.31524688_31524689del	GRCh38
NC_000018.9:g.29104651_29104652del , CM000680.1:g.29104651_29104652del	GRCh37
NC_000018.8:g.27358649_27358650del	NCBI36
NG_007072.3:g.31447_31448del , LRG_397:g.31447_31448del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682087.2:n.660-15_660-14del
ENST00000683614.2:n.660-15_660-14del
ENST00000682087.1:c.660-15_660-14del
ENST00000683614.1:c.660-15_660-14del
ENST00000261590.13:c.829-15_829-14del MANE Select	ENSP00000261590.8:n.829-15_829-14del
ENST00000261590.12:c.829-15_829-14del	ENSP00000261590.8:n.829-15_829-14del
NM_001943.3:c.829-15_829-14del , LRG_397t1:c.829-15_829-14del	NP_001934.2:n.829-15_829-14del
NM_001943.4:c.829-15_829-14del	NP_001934.2:n.829-15_829-14del
XM_024451095.1:c.295-15_295-14del	XP_024306863.1:n.295-15_295-14del
NM_001943.5:c.829-15_829-14del MANE Select	NP_001934.2:n.829-15_829-14del