Canonical Allele Identifier: CA038745
Gene: DSC2 HGNC NCBI

Linked Data

dbSNP Id: rs754328254

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31089554G>A , CM000680.2:g.31089554G>A GRCh38
NC_000018.9:g.28669517G>A , CM000680.1:g.28669517G>A GRCh37
NC_000018.8:g.26923515G>A NCBI36
NG_008208.2:g.17872C>T , LRG_400:g.17872C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682357.1:c.86C>T ENSP00000507826.1:p.Ser29Phe
ENST00000251081.8:c.515C>T ENSP00000251081.6:p.Ser172Phe
ENST00000280904.11:c.515C>T MANE Select ENSP00000280904.6:p.Ser172Phe
ENST00000648081.1:c.86C>T ENSP00000497441.1:p.Ser29Phe
ENST00000251081.6:c.515C>T ENSP00000251081.6:p.Ser172Phe
ENST00000280904.10:c.515C>T ENSP00000280904.6:p.Ser172Phe
NM_004949.4:c.515C>T NP_004940.1:p.Ser172Phe
NM_024422.4:c.515C>T NP_077740.1:p.Ser172Phe
XM_005258206.3:c.86C>T XP_005258263.1:p.Ser29Phe
XM_005258206.4:c.86C>T XP_005258263.1:p.Ser29Phe
NM_004949.5:c.515C>T NP_004940.1:p.Ser172Phe
NM_024422.6:c.515C>T MANE Select NP_077740.1:p.Ser172Phe