Canonical Allele Identifier: CA297641626

Gene: DSC2

Linked Data

• dbSNP Id: rs932289309
• gnomAD v2: 18-28669176-GA-G
• gnomAD v3: 18-31089213-GA-G
• gnomAD v4: 18-31089213-GA-G
• MyVariant Identifiers: chr18:g.28669177del (hg19) ; chr18:g.31089214del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31089222del , CM000680.2:g.31089222del	GRCh38
NC_000018.9:g.28669185del , CM000680.1:g.28669185del	GRCh37
NC_000018.8:g.26923183del	NCBI36
NG_008208.2:g.18212del , LRG_400:g.18212del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682357.1:c.201+225del	ENSP00000507826.1:n.201+225del
ENST00000251081.8:c.630+225del	ENSP00000251081.6:n.630+225del
ENST00000280904.11:c.630+225del MANE Select	ENSP00000280904.6:n.630+225del
ENST00000648081.1:c.201+225del	ENSP00000497441.1:n.201+225del
ENST00000251081.6:c.630+225del	ENSP00000251081.6:n.630+225del
ENST00000280904.10:c.630+225del	ENSP00000280904.6:n.630+225del
NM_004949.4:c.630+225del	NP_004940.1:n.630+225del
NM_024422.4:c.630+225del	NP_077740.1:n.630+225del
XM_005258206.3:c.201+225del	XP_005258263.1:n.201+225del
XM_005258206.4:c.201+225del	XP_005258263.1:n.201+225del
NM_004949.5:c.630+225del	NP_004940.1:n.630+225del
NM_024422.6:c.630+225del MANE Select	NP_077740.1:n.630+225del