Canonical Allele Identifier: CA402113690

Gene: DSC2

Linked Data

• ClinVar Variation Id: 3075026
• ClinVar RCV Id: RCV004015552
• MyVariant Identifiers: chr18:g.28669511C>G (hg19) ; chr18:g.31089548C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31089548C>G , CM000680.2:g.31089548C>G	GRCh38
NC_000018.9:g.28669511C>G , CM000680.1:g.28669511C>G	GRCh37
NC_000018.8:g.26923509C>G	NCBI36
NG_008208.2:g.17878G>C , LRG_400:g.17878G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.92G>C	ENSP00000507826.1:p.Arg31Thr
ENST00000251081.8:c.521G>C	ENSP00000251081.6:p.Arg174Thr
ENST00000280904.11:c.521G>C MANE Select	ENSP00000280904.6:p.Arg174Thr
ENST00000648081.1:c.92G>C	ENSP00000497441.1:p.Arg31Thr
ENST00000251081.6:c.521G>C	ENSP00000251081.6:p.Arg174Thr
ENST00000280904.10:c.521G>C	ENSP00000280904.6:p.Arg174Thr
NM_004949.4:c.521G>C	NP_004940.1:p.Arg174Thr
NM_024422.4:c.521G>C	NP_077740.1:p.Arg174Thr
XM_005258206.3:c.92G>C	XP_005258263.1:p.Arg31Thr
XM_005258206.4:c.92G>C	XP_005258263.1:p.Arg31Thr
NM_004949.5:c.521G>C	NP_004940.1:p.Arg174Thr
NM_024422.6:c.521G>C MANE Select	NP_077740.1:p.Arg174Thr