Canonical Allele Identifier: CA2293645123

Gene: DSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31067323T= , CM000680.2:g.31067323T=	GRCh38
NC_000018.9:g.28647289T= , CM000680.1:g.28647289T=	GRCh37
NC_000018.8:g.26901287T=	NCBI36
NG_008208.2:g.40103A= , LRG_400:g.40103A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.*692A=	ENSP00000507826.1:n.*692A=
ENST00000251081.8:c.*900A=	ENSP00000251081.6:n.*900A=
ENST00000280904.11:c.*692A= MANE Select	ENSP00000280904.6:n.*692A=
ENST00000648081.1:c.*692A=	ENSP00000497441.1:n.*692A=
ENST00000251081.6:c.*900A=	ENSP00000251081.6:n.*900A=
ENST00000280904.10:c.*692A=	ENSP00000280904.6:n.*692A=
NM_004949.4:c.*900A=	NP_004940.1:n.*900A=
NM_024422.4:c.*692A=	NP_077740.1:n.*692A=
XM_005258206.3:c.*692A=	XP_005258263.1:n.*692A=
XM_005258206.4:c.*692A=	XP_005258263.1:n.*692A=
NM_004949.5:c.*900A=	NP_004940.1:n.*900A=
NM_024422.6:c.*692A= MANE Select	NP_077740.1:n.*692A=