Canonical Allele Identifier: CA2293646683

Gene: DSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31070814G= , CM000680.2:g.31070814G=	GRCh38
NC_000018.9:g.28650780G= , CM000680.1:g.28650780G=	GRCh37
NC_000018.8:g.26904778G=	NCBI36
NG_008208.2:g.36612C= , LRG_400:g.36612C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.1733C=	ENSP00000507826.1:p.Thr578=
ENST00000251081.8:c.2162C=	ENSP00000251081.6:p.Thr721=
ENST00000280904.11:c.2162C= MANE Select	ENSP00000280904.6:p.Thr721=
ENST00000648081.1:c.1733C=	ENSP00000497441.1:p.Thr578=
ENST00000251081.6:c.2162C=	ENSP00000251081.6:p.Thr721=
ENST00000280904.10:c.2162C=	ENSP00000280904.6:p.Thr721=
NM_004949.4:c.2162C=	NP_004940.1:p.Thr721=
NM_024422.4:c.2162C=	NP_077740.1:p.Thr721=
XM_005258206.3:c.1733C=	XP_005258263.1:p.Thr578=
XM_005258206.4:c.1733C=	XP_005258263.1:p.Thr578=
NM_004949.5:c.2162C=	NP_004940.1:p.Thr721=
NM_024422.6:c.2162C= MANE Select	NP_077740.1:p.Thr721=