Canonical Allele Identifier: CA2293645090

Gene: DSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31067267C= , CM000680.2:g.31067267C=	GRCh38
NC_000018.9:g.28647233C= , CM000680.1:g.28647233C=	GRCh37
NC_000018.8:g.26901231C=	NCBI36
NG_008208.2:g.40159G= , LRG_400:g.40159G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.*748G=	ENSP00000507826.1:n.*748G=
ENST00000251081.8:c.*956G=	ENSP00000251081.6:n.*956G=
ENST00000280904.11:c.*748G= MANE Select	ENSP00000280904.6:n.*748G=
ENST00000648081.1:c.*748G=	ENSP00000497441.1:n.*748G=
ENST00000251081.6:c.*956G=	ENSP00000251081.6:n.*956G=
ENST00000280904.10:c.*748G=	ENSP00000280904.6:n.*748G=
NM_004949.4:c.*956G=	NP_004940.1:n.*956G=
NM_024422.4:c.*748G=	NP_077740.1:n.*748G=
XM_005258206.3:c.*748G=	XP_005258263.1:n.*748G=
XM_005258206.4:c.*748G=	XP_005258263.1:n.*748G=
NM_004949.5:c.*956G=	NP_004940.1:n.*956G=
NM_024422.6:c.*748G= MANE Select	NP_077740.1:n.*748G=