Canonical Allele Identifier: CA2293646559

Gene: DSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31070532A= , CM000680.2:g.31070532A=	GRCh38
NC_000018.9:g.28650498A= , CM000680.1:g.28650498A=	GRCh37
NC_000018.8:g.26904496A=	NCBI36
NG_008208.2:g.36894T= , LRG_400:g.36894T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.1821+194T=	ENSP00000507826.1:n.1821+194T=
ENST00000251081.8:c.2250+194T=	ENSP00000251081.6:n.2250+194T=
ENST00000280904.11:c.2250+194T= MANE Select	ENSP00000280904.6:n.2250+194T=
ENST00000648081.1:c.1821+194T=	ENSP00000497441.1:n.1821+194T=
ENST00000251081.6:c.2250+194T=	ENSP00000251081.6:n.2250+194T=
ENST00000280904.10:c.2250+194T=	ENSP00000280904.6:n.2250+194T=
NM_004949.4:c.2250+194T=	NP_004940.1:n.2250+194T=
NM_024422.4:c.2250+194T=	NP_077740.1:n.2250+194T=
XM_005258206.3:c.1821+194T=	XP_005258263.1:n.1821+194T=
XM_005258206.4:c.1821+194T=	XP_005258263.1:n.1821+194T=
NM_004949.5:c.2250+194T=	NP_004940.1:n.2250+194T=
NM_024422.6:c.2250+194T= MANE Select	NP_077740.1:n.2250+194T=