Canonical Allele Identifier: CA402147171

Gene: DSG2 DSG2-AS1

Linked Data

• dbSNP Id: rs768724147
• MyVariant Identifiers: chr18:g.29126216G>T (hg19) ; chr18:g.31546253G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31546253G>T , CM000680.2:g.31546253G>T	GRCh38
NC_000018.9:g.29126216G>T , CM000680.1:g.29126216G>T	GRCh37
NC_000018.8:g.27380214G>T	NCBI36
NG_007072.3:g.53012G>T , LRG_397:g.53012G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261590.13:c.2867G>T (DSG2) MANE Select	ENSP00000261590.8:p.Ser956Ile
ENST00000261590.12:c.2867G>T (DSG2)	ENSP00000261590.8:p.Ser956Ile
NM_001943.3:c.2867G>T , LRG_397t1:c.2867G>T (DSG2)	NP_001934.2:p.Ser956Ile
NR_045216.1:n.1346-347C>A (DSG2-AS1)
NM_001943.4:c.2867G>T (DSG2)	NP_001934.2:p.Ser956Ile
XM_024451095.1:c.2333G>T (DSG2)	XP_024306863.1:p.Ser778Ile
NM_001943.5:c.2867G>T (DSG2) MANE Select	NP_001934.2:p.Ser956Ile