Canonical Allele Identifier: CA046150

Gene: DSP

Linked Data

• ClinVar Variation Id: 573062
• ClinVar RCV Id: RCV000694629 ; RCV001191951 ; RCV002477576 ; RCV003999620 ; RCV004025209
• dbSNP Id: rs759443302
• ExAC: 6:7583454 G / A
• gnomAD v2: 6-7583454-G-A
• gnomAD v3: 6-7583221-G-A
• gnomAD v4: 6-7583221-G-A
• MyVariant Identifiers: chr6:g.7583454G>A (hg19) ; chr6:g.7583221G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583221G>A , CM000668.2:g.7583221G>A	GRCh38
NC_000006.11:g.7583454G>A , CM000668.1:g.7583454G>A	GRCh37
NC_000006.10:g.7528453G>A	NCBI36
NG_008803.1:g.46585G>A , LRG_423:g.46585G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.4630G>A	ENSP00000518230.1:p.Asp1544Asn
ENST00000379802.8:c.5959G>A MANE Select	ENSP00000369129.3:p.Asp1987Asn
ENST00000379802.7:c.5959G>A	ENSP00000369129.3:p.Asp1987Asn
ENST00000418664.2:c.4162G>A	ENSP00000396591.2:p.Asp1388Asn
NM_001008844.1:c.4162G>A	NP_001008844.1:p.Asp1388Asn
NM_004415.2:c.5959G>A , LRG_423t1:c.5959G>A	NP_004406.2:p.Asp1987Asn
XM_011514323.1:c.4630G>A	XP_011512625.1:p.Asp1544Asn
NM_001008844.2:c.4162G>A	NP_001008844.1:p.Asp1388Asn
NM_001319034.1:c.4630G>A	NP_001305963.1:p.Asp1544Asn
NM_004415.3:c.5959G>A	NP_004406.2:p.Asp1987Asn
NM_004415.4:c.5959G>A MANE Select	NP_004406.2:p.Asp1987Asn
NM_001008844.3:c.4162G>A	NP_001008844.1:p.Asp1388Asn
NM_001319034.2:c.4630G>A	NP_001305963.1:p.Asp1544Asn