Canonical Allele Identifier: CA16615761

Gene: DSC2

Linked Data

• ClinVar Variation Id: 410646
• ClinVar RCV Id: RCV000474033 ; RCV004001862
• dbSNP Id: rs1060502988
• MyVariant Identifiers: chr18:g.28648004C>T (hg19) ; chr18:g.31068038C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31068038C>T , CM000680.2:g.31068038C>T	GRCh38
NC_000018.9:g.28648004C>T , CM000680.1:g.28648004C>T	GRCh37
NC_000018.8:g.26902002C>T	NCBI36
NG_008208.2:g.39388G>A , LRG_400:g.39388G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.2254G>A	ENSP00000507826.1:p.Ala752Thr
ENST00000251081.8:c.*185G>A	ENSP00000251081.6:n.*185G>A
ENST00000280904.11:c.2683G>A MANE Select	ENSP00000280904.6:p.Ala895Thr
ENST00000648081.1:c.2254G>A	ENSP00000497441.1:p.Ala752Thr
ENST00000251081.6:c.*185G>A	ENSP00000251081.6:n.*185G>A
ENST00000280904.10:c.2683G>A	ENSP00000280904.6:p.Ala895Thr
NM_004949.4:c.*185G>A	NP_004940.1:n.*185G>A
NM_024422.4:c.2683G>A	NP_077740.1:p.Ala895Thr
XM_005258206.3:c.2254G>A	XP_005258263.1:p.Ala752Thr
XM_005258206.4:c.2254G>A	XP_005258263.1:p.Ala752Thr
NM_004949.5:c.*185G>A	NP_004940.1:n.*185G>A
NM_024422.6:c.2683G>A MANE Select	NP_077740.1:p.Ala895Thr