Canonical Allele Identifier: CA2293645114

Gene: DSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31067302G= , CM000680.2:g.31067302G=	GRCh38
NC_000018.9:g.28647268G= , CM000680.1:g.28647268G=	GRCh37
NC_000018.8:g.26901266G=	NCBI36
NG_008208.2:g.40124C= , LRG_400:g.40124C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.*713C=	ENSP00000507826.1:n.*713C=
ENST00000251081.8:c.*921C=	ENSP00000251081.6:n.*921C=
ENST00000280904.11:c.*713C= MANE Select	ENSP00000280904.6:n.*713C=
ENST00000648081.1:c.*713C=	ENSP00000497441.1:n.*713C=
ENST00000251081.6:c.*921C=	ENSP00000251081.6:n.*921C=
ENST00000280904.10:c.*713C=	ENSP00000280904.6:n.*713C=
NM_004949.4:c.*921C=	NP_004940.1:n.*921C=
NM_024422.4:c.*713C=	NP_077740.1:n.*713C=
XM_005258206.3:c.*713C=	XP_005258263.1:n.*713C=
XM_005258206.4:c.*713C=	XP_005258263.1:n.*713C=
NM_004949.5:c.*921C=	NP_004940.1:n.*921C=
NM_024422.6:c.*713C= MANE Select	NP_077740.1:n.*713C=