Canonical Allele Identifier: CA362695152

Gene: DSP

Linked Data

• ClinVar Variation Id: 942088
• ClinVar RCV Id: RCV001212001 ; RCV002411781
• dbSNP Id: rs1303168294
• gnomAD v4: 6-7585702-C-A
• MyVariant Identifiers: chr6:g.7585935C>A (hg19) ; chr6:g.7585702C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585702C>A , CM000668.2:g.7585702C>A	GRCh38
NC_000006.11:g.7585935C>A , CM000668.1:g.7585935C>A	GRCh37
NC_000006.10:g.7530934C>A	NCBI36
NG_008803.1:g.49066C>A , LRG_423:g.49066C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.7111C>A	ENSP00000518230.1:p.Pro2371Thr
ENST00000379802.8:c.8440C>A MANE Select	ENSP00000369129.3:p.Pro2814Thr
ENST00000379802.7:c.8440C>A	ENSP00000369129.3:p.Pro2814Thr
ENST00000418664.2:c.6643C>A	ENSP00000396591.2:p.Pro2215Thr
NM_001008844.1:c.6643C>A	NP_001008844.1:p.Pro2215Thr
NM_004415.2:c.8440C>A , LRG_423t1:c.8440C>A	NP_004406.2:p.Pro2814Thr
XM_011514323.1:c.7111C>A	XP_011512625.1:p.Pro2371Thr
NM_001008844.2:c.6643C>A	NP_001008844.1:p.Pro2215Thr
NM_001319034.1:c.7111C>A	NP_001305963.1:p.Pro2371Thr
NM_004415.3:c.8440C>A	NP_004406.2:p.Pro2814Thr
NM_004415.4:c.8440C>A MANE Select	NP_004406.2:p.Pro2814Thr
NM_001008844.3:c.6643C>A	NP_001008844.1:p.Pro2215Thr
NM_001319034.2:c.7111C>A	NP_001305963.1:p.Pro2371Thr