Canonical Allele Identifier: CA362684512

Gene: DSP

Linked Data

• ClinVar Variation Id: 925677
• ClinVar RCV Id: RCV001187762
• dbSNP Id: rs1759362068
• gnomAD v4: 6-7579823-A-C
• MyVariant Identifiers: chr6:g.7580056A>C (hg19) ; chr6:g.7579823A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7579823A>C , CM000668.2:g.7579823A>C	GRCh38
NC_000006.11:g.7580056A>C , CM000668.1:g.7580056A>C	GRCh37
NC_000006.10:g.7525055A>C	NCBI36
NG_008803.1:g.43187A>C , LRG_423:g.43187A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000710359.1:c.3633A>C	ENSP00000518230.1:p.Glu1211Asp
ENST00000379802.8:c.3633A>C MANE Select	ENSP00000369129.3:p.Glu1211Asp
ENST00000379802.7:c.3633A>C	ENSP00000369129.3:p.Glu1211Asp
ENST00000418664.2:c.3582+51A>C	ENSP00000396591.2:n.3582+51A>C
NM_001008844.1:c.3582+51A>C	NP_001008844.1:n.3582+51A>C
NM_004415.2:c.3633A>C , LRG_423t1:c.3633A>C	NP_004406.2:p.Glu1211Asp
XM_011514323.1:c.3633A>C	XP_011512625.1:p.Glu1211Asp
NM_001008844.2:c.3582+51A>C	NP_001008844.1:n.3582+51A>C
NM_001319034.1:c.3633A>C	NP_001305963.1:p.Glu1211Asp
NM_004415.3:c.3633A>C	NP_004406.2:p.Glu1211Asp
NM_004415.4:c.3633A>C MANE Select	NP_004406.2:p.Glu1211Asp
NM_001008844.3:c.3582+51A>C	NP_001008844.1:n.3582+51A>C
NM_001319034.2:c.3633A>C	NP_001305963.1:p.Glu1211Asp