Canonical Allele Identifier: CA2560462431
Gene: DSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31067360G>A , CM000680.2:g.31067360G>A GRCh38
NC_000018.9:g.28647326G>A , CM000680.1:g.28647326G>A GRCh37
NC_000018.8:g.26901324G>A NCBI36
NG_008208.2:g.40066C>T , LRG_400:g.40066C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682357.1:c.*655C>T ENSP00000507826.1:n.*655C>T
ENST00000251081.8:c.*863C>T ENSP00000251081.6:n.*863C>T
ENST00000280904.11:c.*655C>T MANE Select ENSP00000280904.6:n.*655C>T
ENST00000648081.1:c.*655C>T ENSP00000497441.1:n.*655C>T
ENST00000251081.6:c.*863C>T ENSP00000251081.6:n.*863C>T
ENST00000280904.10:c.*655C>T ENSP00000280904.6:n.*655C>T
NM_004949.4:c.*863C>T NP_004940.1:n.*863C>T
NM_024422.4:c.*655C>T NP_077740.1:n.*655C>T
XM_005258206.3:c.*655C>T XP_005258263.1:n.*655C>T
XM_005258206.4:c.*655C>T XP_005258263.1:n.*655C>T
NM_004949.5:c.*863C>T NP_004940.1:n.*863C>T
NM_024422.6:c.*655C>T MANE Select NP_077740.1:n.*655C>T