Canonical Allele Identifier: CA362694060

Gene: DSP

Linked Data

• ClinVar Variation Id: 915496
• ClinVar RCV Id: RCV001170148 ; RCV001664723
• dbSNP Id: rs1759606289
• gnomAD v4: 6-7585181-G-A
• MyVariant Identifiers: chr6:g.7585414G>A (hg19) ; chr6:g.7585181G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585181G>A , CM000668.2:g.7585181G>A	GRCh38
NC_000006.11:g.7585414G>A , CM000668.1:g.7585414G>A	GRCh37
NC_000006.10:g.7530413G>A	NCBI36
NG_008803.1:g.48545G>A , LRG_423:g.48545G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6590G>A	ENSP00000518230.1:p.Gly2197Asp
ENST00000379802.8:c.7919G>A MANE Select	ENSP00000369129.3:p.Gly2640Asp
ENST00000379802.7:c.7919G>A	ENSP00000369129.3:p.Gly2640Asp
ENST00000418664.2:c.6122G>A	ENSP00000396591.2:p.Gly2041Asp
NM_001008844.1:c.6122G>A	NP_001008844.1:p.Gly2041Asp
NM_004415.2:c.7919G>A , LRG_423t1:c.7919G>A	NP_004406.2:p.Gly2640Asp
XM_011514323.1:c.6590G>A	XP_011512625.1:p.Gly2197Asp
NM_001008844.2:c.6122G>A	NP_001008844.1:p.Gly2041Asp
NM_001319034.1:c.6590G>A	NP_001305963.1:p.Gly2197Asp
NM_004415.3:c.7919G>A	NP_004406.2:p.Gly2640Asp
NM_004415.4:c.7919G>A MANE Select	NP_004406.2:p.Gly2640Asp
NM_001008844.3:c.6122G>A	NP_001008844.1:p.Gly2041Asp
NM_001319034.2:c.6590G>A	NP_001305963.1:p.Gly2197Asp