Canonical Allele Identifier: CA402112478

Gene: DSC2

Linked Data

• COSMIC: COSM6003378 ; COSM6003379
• MyVariant Identifiers: chr18:g.28650759A>T (hg19) ; chr18:g.31070793A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31070793A>T , CM000680.2:g.31070793A>T	GRCh38
NC_000018.9:g.28650759A>T , CM000680.1:g.28650759A>T	GRCh37
NC_000018.8:g.26904757A>T	NCBI36
NG_008208.2:g.36633T>A , LRG_400:g.36633T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.1754T>A	ENSP00000507826.1:p.Ile585Asn
ENST00000251081.8:c.2183T>A	ENSP00000251081.6:p.Ile728Asn
ENST00000280904.11:c.2183T>A MANE Select	ENSP00000280904.6:p.Ile728Asn
ENST00000648081.1:c.1754T>A	ENSP00000497441.1:p.Ile585Asn
ENST00000251081.6:c.2183T>A	ENSP00000251081.6:p.Ile728Asn
ENST00000280904.10:c.2183T>A	ENSP00000280904.6:p.Ile728Asn
NM_004949.4:c.2183T>A	NP_004940.1:p.Ile728Asn
NM_024422.4:c.2183T>A	NP_077740.1:p.Ile728Asn
XM_005258206.3:c.1754T>A	XP_005258263.1:p.Ile585Asn
XM_005258206.4:c.1754T>A	XP_005258263.1:p.Ile585Asn
NM_004949.5:c.2183T>A	NP_004940.1:p.Ile728Asn
NM_024422.6:c.2183T>A MANE Select	NP_077740.1:p.Ile728Asn