Canonical Allele Identifier: CA402113556

Gene: DSC2

Linked Data

• gnomAD v4: 18-31089495-T-C
• MyVariant Identifiers: chr18:g.28669458T>C (hg19) ; chr18:g.31089495T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31089495T>C , CM000680.2:g.31089495T>C	GRCh38
NC_000018.9:g.28669458T>C , CM000680.1:g.28669458T>C	GRCh37
NC_000018.8:g.26923456T>C	NCBI36
NG_008208.2:g.17931A>G , LRG_400:g.17931A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.145A>G	ENSP00000507826.1:p.Thr49Ala
ENST00000251081.8:c.574A>G	ENSP00000251081.6:p.Thr192Ala
ENST00000280904.11:c.574A>G MANE Select	ENSP00000280904.6:p.Thr192Ala
ENST00000648081.1:c.145A>G	ENSP00000497441.1:p.Thr49Ala
ENST00000251081.6:c.574A>G	ENSP00000251081.6:p.Thr192Ala
ENST00000280904.10:c.574A>G	ENSP00000280904.6:p.Thr192Ala
NM_004949.4:c.574A>G	NP_004940.1:p.Thr192Ala
NM_024422.4:c.574A>G	NP_077740.1:p.Thr192Ala
XM_005258206.3:c.145A>G	XP_005258263.1:p.Thr49Ala
XM_005258206.4:c.145A>G	XP_005258263.1:p.Thr49Ala
NM_004949.5:c.574A>G	NP_004940.1:p.Thr192Ala
NM_024422.6:c.574A>G MANE Select	NP_077740.1:p.Thr192Ala