Canonical Allele Identifier: CA2293654786

Gene: DSC2

Linked Data

• dbSNP Id: rs1987503854

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31089182_31089183insTAA , CM000680.2:g.31089182_31089183insTAA	GRCh38
NC_000018.9:g.28669145_28669146insTAA , CM000680.1:g.28669145_28669146insTAA	GRCh37
NC_000018.8:g.26923143_26923144insTAA	NCBI36
NG_008208.2:g.18245_18246insATT , LRG_400:g.18245_18246insATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.201+258_201+259insATT	ENSP00000507826.1:n.201+258_201+259insATT
ENST00000251081.8:c.630+258_630+259insATT	ENSP00000251081.6:n.630+258_630+259insATT
ENST00000280904.11:c.630+258_630+259insATT MANE Select	ENSP00000280904.6:n.630+258_630+259insATT
ENST00000648081.1:c.201+258_201+259insATT	ENSP00000497441.1:n.201+258_201+259insATT
ENST00000251081.6:c.630+258_630+259insATT	ENSP00000251081.6:n.630+258_630+259insATT
ENST00000280904.10:c.630+258_630+259insATT	ENSP00000280904.6:n.630+258_630+259insATT
NM_004949.4:c.630+258_630+259insATT	NP_004940.1:n.630+258_630+259insATT
NM_024422.4:c.630+258_630+259insATT	NP_077740.1:n.630+258_630+259insATT
XM_005258206.3:c.201+258_201+259insATT	XP_005258263.1:n.201+258_201+259insATT
XM_005258206.4:c.201+258_201+259insATT	XP_005258263.1:n.201+258_201+259insATT
NM_004949.5:c.630+258_630+259insATT	NP_004940.1:n.630+258_630+259insATT
NM_024422.6:c.630+258_630+259insATT MANE Select	NP_077740.1:n.630+258_630+259insATT