Canonical Allele Identifier: CA2293646650

Gene: DSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31070745G= , CM000680.2:g.31070745G=	GRCh38
NC_000018.9:g.28650711G= , CM000680.1:g.28650711G=	GRCh37
NC_000018.8:g.26904709G=	NCBI36
NG_008208.2:g.36681C= , LRG_400:g.36681C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.1802C=	ENSP00000507826.1:p.Ala601=
ENST00000251081.8:c.2231C=	ENSP00000251081.6:p.Ala744=
ENST00000280904.11:c.2231C= MANE Select	ENSP00000280904.6:p.Ala744=
ENST00000648081.1:c.1802C=	ENSP00000497441.1:p.Ala601=
ENST00000251081.6:c.2231C=	ENSP00000251081.6:p.Ala744=
ENST00000280904.10:c.2231C=	ENSP00000280904.6:p.Ala744=
NM_004949.4:c.2231C=	NP_004940.1:p.Ala744=
NM_024422.4:c.2231C=	NP_077740.1:p.Ala744=
XM_005258206.3:c.1802C=	XP_005258263.1:p.Ala601=
XM_005258206.4:c.1802C=	XP_005258263.1:p.Ala601=
NM_004949.5:c.2231C=	NP_004940.1:p.Ala744=
NM_024422.6:c.2231C= MANE Select	NP_077740.1:p.Ala744=