Canonical Allele Identifier: CA402110504

Gene: DSC2

Linked Data

• ClinVar Variation Id: 629709
• ClinVar RCV Id: RCV000774419
• dbSNP Id: rs1567978310
• MyVariant Identifiers: chr18:g.28662932T>A (hg19) ; chr18:g.31082966T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31082966T>A , CM000680.2:g.31082966T>A	GRCh38
NC_000018.9:g.28662932T>A , CM000680.1:g.28662932T>A	GRCh37
NC_000018.8:g.26916930T>A	NCBI36
NG_008208.2:g.24460A>T , LRG_400:g.24460A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682357.1:c.608A>T	ENSP00000507826.1:p.Asp203Val
ENST00000251081.8:c.1037A>T	ENSP00000251081.6:p.Asp346Val
ENST00000280904.11:c.1037A>T MANE Select	ENSP00000280904.6:p.Asp346Val
ENST00000648081.1:c.608A>T	ENSP00000497441.1:p.Asp203Val
ENST00000251081.6:c.1037A>T	ENSP00000251081.6:p.Asp346Val
ENST00000280904.10:c.1037A>T	ENSP00000280904.6:p.Asp346Val
NM_004949.4:c.1037A>T	NP_004940.1:p.Asp346Val
NM_024422.4:c.1037A>T	NP_077740.1:p.Asp346Val
XM_005258206.3:c.608A>T	XP_005258263.1:p.Asp203Val
XM_005258206.4:c.608A>T	XP_005258263.1:p.Asp203Val
NM_004949.5:c.1037A>T	NP_004940.1:p.Asp346Val
NM_024422.6:c.1037A>T MANE Select	NP_077740.1:p.Asp346Val