Canonical Allele Identifier: CA2641388234

Gene: DSC2

Linked Data

• gnomAD v4: 18-31070874-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31070876_31070877del , CM000680.2:g.31070876_31070877del	GRCh38
NC_000018.9:g.28650842_28650843del , CM000680.1:g.28650842_28650843del	GRCh37
NC_000018.8:g.26904840_26904841del	NCBI36
NG_008208.2:g.36550_36551del , LRG_400:g.36550_36551del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.1697-26_1697-25del	ENSP00000507826.1:n.1697-26_1697-25del
ENST00000251081.8:c.2126-26_2126-25del	ENSP00000251081.6:n.2126-26_2126-25del
ENST00000280904.11:c.2126-26_2126-25del MANE Select	ENSP00000280904.6:n.2126-26_2126-25del
ENST00000648081.1:c.1697-26_1697-25del	ENSP00000497441.1:n.1697-26_1697-25del
ENST00000251081.6:c.2126-26_2126-25del	ENSP00000251081.6:n.2126-26_2126-25del
ENST00000280904.10:c.2126-26_2126-25del	ENSP00000280904.6:n.2126-26_2126-25del
NM_004949.4:c.2126-26_2126-25del	NP_004940.1:n.2126-26_2126-25del
NM_024422.4:c.2126-26_2126-25del	NP_077740.1:n.2126-26_2126-25del
XM_005258206.3:c.1697-26_1697-25del	XP_005258263.1:n.1697-26_1697-25del
XM_005258206.4:c.1697-26_1697-25del	XP_005258263.1:n.1697-26_1697-25del
NM_004949.5:c.2126-26_2126-25del	NP_004940.1:n.2126-26_2126-25del
NM_024422.6:c.2126-26_2126-25del MANE Select	NP_077740.1:n.2126-26_2126-25del