Canonical Allele Identifier: CA913189076

Gene: DSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31070731dup , CM000680.2:g.31070731dup	GRCh38
NC_000018.9:g.28650697dup , CM000680.1:g.28650697dup	GRCh37
NC_000018.8:g.26904695dup	NCBI36
NG_008208.2:g.36697dup , LRG_400:g.36697dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.1818dup	ENSP00000507826.1:p.Val607SerfsTer?
ENST00000251081.8:c.2247dup	ENSP00000251081.6:p.Val750SerfsTer?
ENST00000280904.11:c.2247dup MANE Select	ENSP00000280904.6:p.Val750SerfsTer?
ENST00000648081.1:c.1818dup	ENSP00000497441.1:p.Val607SerfsTer?
ENST00000251081.6:c.2247dup	ENSP00000251081.6:p.Val750SerfsTer?
ENST00000280904.10:c.2247dup	ENSP00000280904.6:p.Val750SerfsTer?
NM_004949.4:c.2247dup	NP_004940.1:p.Val750SerfsTer?
NM_024422.4:c.2247dup	NP_077740.1:p.Val750SerfsTer?
XM_005258206.3:c.1818dup	XP_005258263.1:p.Val607SerfsTer?
XM_005258206.4:c.1818dup	XP_005258263.1:p.Val607SerfsTer?
NM_004949.5:c.2247dup	NP_004940.1:p.Val750SerfsTer?
NM_024422.6:c.2247dup MANE Select	NP_077740.1:p.Val750SerfsTer?