Canonical Allele Identifier: CA503597180

Gene: DSG2

Linked Data

• MyVariant Identifiers: chr18:g.29121265A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31541302A>T , CM000680.2:g.31541302A>T	GRCh38
NC_000018.9:g.29121265A>T , CM000680.1:g.29121265A>T	GRCh37
NC_000018.8:g.27375263A>T	NCBI36
NG_007072.3:g.48061A>T , LRG_397:g.48061A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261590.13:c.1989A>T MANE Select	ENSP00000261590.8:p.Pro663=
ENST00000261590.12:c.1989A>T	ENSP00000261590.8:p.Pro663=
NM_001943.3:c.1989A>T , LRG_397t1:c.1989A>T	NP_001934.2:p.Pro663=
NM_001943.4:c.1989A>T	NP_001934.2:p.Pro663=
XM_024451095.1:c.1455A>T	XP_024306863.1:p.Pro485=
NM_001943.5:c.1989A>T MANE Select	NP_001934.2:p.Pro663=