Canonical Allele Identifier: CA402112338

Gene: DSC2

Linked Data

• MyVariant Identifiers: chr18:g.28650709G>T (hg19) ; chr18:g.31070743G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31070743G>T , CM000680.2:g.31070743G>T	GRCh38
NC_000018.9:g.28650709G>T , CM000680.1:g.28650709G>T	GRCh37
NC_000018.8:g.26904707G>T	NCBI36
NG_008208.2:g.36683C>A , LRG_400:g.36683C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.1804C>A	ENSP00000507826.1:p.Pro602Thr
ENST00000251081.8:c.2233C>A	ENSP00000251081.6:p.Pro745Thr
ENST00000280904.11:c.2233C>A MANE Select	ENSP00000280904.6:p.Pro745Thr
ENST00000648081.1:c.1804C>A	ENSP00000497441.1:p.Pro602Thr
ENST00000251081.6:c.2233C>A	ENSP00000251081.6:p.Pro745Thr
ENST00000280904.10:c.2233C>A	ENSP00000280904.6:p.Pro745Thr
NM_004949.4:c.2233C>A	NP_004940.1:p.Pro745Thr
NM_024422.4:c.2233C>A	NP_077740.1:p.Pro745Thr
XM_005258206.3:c.1804C>A	XP_005258263.1:p.Pro602Thr
XM_005258206.4:c.1804C>A	XP_005258263.1:p.Pro602Thr
NM_004949.5:c.2233C>A	NP_004940.1:p.Pro745Thr
NM_024422.6:c.2233C>A MANE Select	NP_077740.1:p.Pro745Thr