Canonical Allele Identifier: CA2293646601
Gene: DSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31070648G= , CM000680.2:g.31070648G= GRCh38
NC_000018.9:g.28650614G= , CM000680.1:g.28650614G= GRCh37
NC_000018.8:g.26904612G= NCBI36
NG_008208.2:g.36778C= , LRG_400:g.36778C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682357.1:c.1821+78C= ENSP00000507826.1:n.1821+78C=
ENST00000251081.8:c.2250+78C= ENSP00000251081.6:n.2250+78C=
ENST00000280904.11:c.2250+78C= MANE Select ENSP00000280904.6:n.2250+78C=
ENST00000648081.1:c.1821+78C= ENSP00000497441.1:n.1821+78C=
ENST00000251081.6:c.2250+78C= ENSP00000251081.6:n.2250+78C=
ENST00000280904.10:c.2250+78C= ENSP00000280904.6:n.2250+78C=
NM_004949.4:c.2250+78C= NP_004940.1:n.2250+78C=
NM_024422.4:c.2250+78C= NP_077740.1:n.2250+78C=
XM_005258206.3:c.1821+78C= XP_005258263.1:n.1821+78C=
XM_005258206.4:c.1821+78C= XP_005258263.1:n.1821+78C=
NM_004949.5:c.2250+78C= NP_004940.1:n.2250+78C=
NM_024422.6:c.2250+78C= MANE Select NP_077740.1:n.2250+78C=