Canonical Allele Identifier: CA402112347

Gene: DSC2

Linked Data

• ClinVar Variation Id: 3075452
• ClinVar RCV Id: RCV004016970
• MyVariant Identifiers: chr18:g.28650712C>A (hg19) ; chr18:g.31070746C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31070746C>A , CM000680.2:g.31070746C>A	GRCh38
NC_000018.9:g.28650712C>A , CM000680.1:g.28650712C>A	GRCh37
NC_000018.8:g.26904710C>A	NCBI36
NG_008208.2:g.36680G>T , LRG_400:g.36680G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.1801G>T	ENSP00000507826.1:p.Ala601Ser
ENST00000251081.8:c.2230G>T	ENSP00000251081.6:p.Ala744Ser
ENST00000280904.11:c.2230G>T MANE Select	ENSP00000280904.6:p.Ala744Ser
ENST00000648081.1:c.1801G>T	ENSP00000497441.1:p.Ala601Ser
ENST00000251081.6:c.2230G>T	ENSP00000251081.6:p.Ala744Ser
ENST00000280904.10:c.2230G>T	ENSP00000280904.6:p.Ala744Ser
NM_004949.4:c.2230G>T	NP_004940.1:p.Ala744Ser
NM_024422.4:c.2230G>T	NP_077740.1:p.Ala744Ser
XM_005258206.3:c.1801G>T	XP_005258263.1:p.Ala601Ser
XM_005258206.4:c.1801G>T	XP_005258263.1:p.Ala601Ser
NM_004949.5:c.2230G>T	NP_004940.1:p.Ala744Ser
NM_024422.6:c.2230G>T MANE Select	NP_077740.1:p.Ala744Ser