Canonical Allele Identifier: CA2293646606
Gene: DSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31070661T= , CM000680.2:g.31070661T= GRCh38
NC_000018.9:g.28650627T= , CM000680.1:g.28650627T= GRCh37
NC_000018.8:g.26904625T= NCBI36
NG_008208.2:g.36765A= , LRG_400:g.36765A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682357.1:c.1821+65A= ENSP00000507826.1:n.1821+65A=
ENST00000251081.8:c.2250+65A= ENSP00000251081.6:n.2250+65A=
ENST00000280904.11:c.2250+65A= MANE Select ENSP00000280904.6:n.2250+65A=
ENST00000648081.1:c.1821+65A= ENSP00000497441.1:n.1821+65A=
ENST00000251081.6:c.2250+65A= ENSP00000251081.6:n.2250+65A=
ENST00000280904.10:c.2250+65A= ENSP00000280904.6:n.2250+65A=
NM_004949.4:c.2250+65A= NP_004940.1:n.2250+65A=
NM_024422.4:c.2250+65A= NP_077740.1:n.2250+65A=
XM_005258206.3:c.1821+65A= XP_005258263.1:n.1821+65A=
XM_005258206.4:c.1821+65A= XP_005258263.1:n.1821+65A=
NM_004949.5:c.2250+65A= NP_004940.1:n.2250+65A=
NM_024422.6:c.2250+65A= MANE Select NP_077740.1:n.2250+65A=