Canonical Allele Identifier: CA448531289

Gene: DSP

Linked Data

• ClinVar Variation Id: 2940273
• ClinVar RCV Id: RCV003797631
• gnomAD v4: 6-7585806-A-T
• MyVariant Identifiers: chr6:g.7586039A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585806A>T , CM000668.2:g.7585806A>T	GRCh38
NC_000006.11:g.7586039A>T , CM000668.1:g.7586039A>T	GRCh37
NC_000006.10:g.7531038A>T	NCBI36
NG_008803.1:g.49170A>T , LRG_423:g.49170A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.7215A>T	ENSP00000518230.1:p.Gly2405=
ENST00000379802.8:c.8544A>T MANE Select	ENSP00000369129.3:p.Gly2848=
ENST00000379802.7:c.8544A>T	ENSP00000369129.3:p.Gly2848=
ENST00000418664.2:c.6747A>T	ENSP00000396591.2:p.Gly2249=
NM_001008844.1:c.6747A>T	NP_001008844.1:p.Gly2249=
NM_004415.2:c.8544A>T , LRG_423t1:c.8544A>T	NP_004406.2:p.Gly2848=
XM_011514323.1:c.7215A>T	XP_011512625.1:p.Gly2405=
NM_001008844.2:c.6747A>T	NP_001008844.1:p.Gly2249=
NM_001319034.1:c.7215A>T	NP_001305963.1:p.Gly2405=
NM_004415.3:c.8544A>T	NP_004406.2:p.Gly2848=
NM_004415.4:c.8544A>T MANE Select	NP_004406.2:p.Gly2848=
NM_001008844.3:c.6747A>T	NP_001008844.1:p.Gly2249=
NM_001319034.2:c.7215A>T	NP_001305963.1:p.Gly2405=