Canonical Allele Identifier: CA2641384261

Gene: DSC2

Linked Data

• gnomAD v4: 18-31067297-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31067297A>G , CM000680.2:g.31067297A>G	GRCh38
NC_000018.9:g.28647263A>G , CM000680.1:g.28647263A>G	GRCh37
NC_000018.8:g.26901261A>G	NCBI36
NG_008208.2:g.40129T>C , LRG_400:g.40129T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.*718T>C	ENSP00000507826.1:n.*718T>C
ENST00000251081.8:c.*926T>C	ENSP00000251081.6:n.*926T>C
ENST00000280904.11:c.*718T>C MANE Select	ENSP00000280904.6:n.*718T>C
ENST00000648081.1:c.*718T>C	ENSP00000497441.1:n.*718T>C
ENST00000251081.6:c.*926T>C	ENSP00000251081.6:n.*926T>C
ENST00000280904.10:c.*718T>C	ENSP00000280904.6:n.*718T>C
NM_004949.4:c.*926T>C	NP_004940.1:n.*926T>C
NM_024422.4:c.*718T>C	NP_077740.1:n.*718T>C
XM_005258206.3:c.*718T>C	XP_005258263.1:n.*718T>C
XM_005258206.4:c.*718T>C	XP_005258263.1:n.*718T>C
NM_004949.5:c.*926T>C	NP_004940.1:n.*926T>C
NM_024422.6:c.*718T>C MANE Select	NP_077740.1:n.*718T>C