Canonical Allele Identifier: CA362693599

Gene: DSP

Linked Data

• ClinVar Variation Id: 2931014
• ClinVar RCV Id: RCV003782276
• gnomAD v4: 6-7584968-C-A
• MyVariant Identifiers: chr6:g.7585201C>A (hg19) ; chr6:g.7584968C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7584968C>A , CM000668.2:g.7584968C>A	GRCh38
NC_000006.11:g.7585201C>A , CM000668.1:g.7585201C>A	GRCh37
NC_000006.10:g.7530200C>A	NCBI36
NG_008803.1:g.48332C>A , LRG_423:g.48332C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6377C>A	ENSP00000518230.1:p.Thr2126Asn
ENST00000379802.8:c.7706C>A MANE Select	ENSP00000369129.3:p.Thr2569Asn
ENST00000379802.7:c.7706C>A	ENSP00000369129.3:p.Thr2569Asn
ENST00000418664.2:c.5909C>A	ENSP00000396591.2:p.Thr1970Asn
NM_001008844.1:c.5909C>A	NP_001008844.1:p.Thr1970Asn
NM_004415.2:c.7706C>A , LRG_423t1:c.7706C>A	NP_004406.2:p.Thr2569Asn
XM_011514323.1:c.6377C>A	XP_011512625.1:p.Thr2126Asn
NM_001008844.2:c.5909C>A	NP_001008844.1:p.Thr1970Asn
NM_001319034.1:c.6377C>A	NP_001305963.1:p.Thr2126Asn
NM_004415.3:c.7706C>A	NP_004406.2:p.Thr2569Asn
NM_004415.4:c.7706C>A MANE Select	NP_004406.2:p.Thr2569Asn
NM_001008844.3:c.5909C>A	NP_001008844.1:p.Thr1970Asn
NM_001319034.2:c.6377C>A	NP_001305963.1:p.Thr2126Asn