Canonical Allele Identifier: CA051221

Gene: DSP

Linked Data

• ClinVar Variation Id: 3073414
• ClinVar RCV Id: RCV004016420
• dbSNP Id: rs759771417
• ExAC: 6:7585451 G / A
• gnomAD v2: 6-7585451-G-A
• gnomAD v3: 6-7585218-G-A
• gnomAD v4: 6-7585218-G-A
• MyVariant Identifiers: chr6:g.7585451G>A (hg19) ; chr6:g.7585218G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585218G>A , CM000668.2:g.7585218G>A	GRCh38
NC_000006.11:g.7585451G>A , CM000668.1:g.7585451G>A	GRCh37
NC_000006.10:g.7530450G>A	NCBI36
NG_008803.1:g.48582G>A , LRG_423:g.48582G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6627G>A	ENSP00000518230.1:p.Glu2209=
ENST00000379802.8:c.7956G>A MANE Select	ENSP00000369129.3:p.Glu2652=
ENST00000379802.7:c.7956G>A	ENSP00000369129.3:p.Glu2652=
ENST00000418664.2:c.6159G>A	ENSP00000396591.2:p.Glu2053=
NM_001008844.1:c.6159G>A	NP_001008844.1:p.Glu2053=
NM_004415.2:c.7956G>A , LRG_423t1:c.7956G>A	NP_004406.2:p.Glu2652=
XM_011514323.1:c.6627G>A	XP_011512625.1:p.Glu2209=
NM_001008844.2:c.6159G>A	NP_001008844.1:p.Glu2053=
NM_001319034.1:c.6627G>A	NP_001305963.1:p.Glu2209=
NM_004415.3:c.7956G>A	NP_004406.2:p.Glu2652=
NM_004415.4:c.7956G>A MANE Select	NP_004406.2:p.Glu2652=
NM_001008844.3:c.6159G>A	NP_001008844.1:p.Glu2053=
NM_001319034.2:c.6627G>A	NP_001305963.1:p.Glu2209=