Canonical Allele Identifier: CA402113312

Gene: DSC2

Linked Data

• MyVariant Identifiers: chr18:g.28669404C>A (hg19) ; chr18:g.31089441C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31089441C>A , CM000680.2:g.31089441C>A	GRCh38
NC_000018.9:g.28669404C>A , CM000680.1:g.28669404C>A	GRCh37
NC_000018.8:g.26923402C>A	NCBI36
NG_008208.2:g.17985G>T , LRG_400:g.17985G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.199G>T	ENSP00000507826.1:p.Glu67Ter
ENST00000251081.8:c.628G>T	ENSP00000251081.6:p.Glu210Ter
ENST00000280904.11:c.628G>T MANE Select	ENSP00000280904.6:p.Glu210Ter
ENST00000648081.1:c.199G>T	ENSP00000497441.1:p.Glu67Ter
ENST00000251081.6:c.628G>T	ENSP00000251081.6:p.Glu210Ter
ENST00000280904.10:c.628G>T	ENSP00000280904.6:p.Glu210Ter
NM_004949.4:c.628G>T	NP_004940.1:p.Glu210Ter
NM_024422.4:c.628G>T	NP_077740.1:p.Glu210Ter
XM_005258206.3:c.199G>T	XP_005258263.1:p.Glu67Ter
XM_005258206.4:c.199G>T	XP_005258263.1:p.Glu67Ter
NM_004949.5:c.628G>T	NP_004940.1:p.Glu210Ter
NM_024422.6:c.628G>T MANE Select	NP_077740.1:p.Glu210Ter