Canonical Allele Identifier: CA362693898

Gene: DSP

Linked Data

• dbSNP Id: rs1221504284
• gnomAD v2: 6-7585338-G-A
• gnomAD v4: 6-7585105-G-A
• MyVariant Identifiers: chr6:g.7585338G>A (hg19) ; chr6:g.7585105G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585105G>A , CM000668.2:g.7585105G>A	GRCh38
NC_000006.11:g.7585338G>A , CM000668.1:g.7585338G>A	GRCh37
NC_000006.10:g.7530337G>A	NCBI36
NG_008803.1:g.48469G>A , LRG_423:g.48469G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6514G>A	ENSP00000518230.1:p.Glu2172Lys
ENST00000379802.8:c.7843G>A MANE Select	ENSP00000369129.3:p.Glu2615Lys
ENST00000379802.7:c.7843G>A	ENSP00000369129.3:p.Glu2615Lys
ENST00000418664.2:c.6046G>A	ENSP00000396591.2:p.Glu2016Lys
NM_001008844.1:c.6046G>A	NP_001008844.1:p.Glu2016Lys
NM_004415.2:c.7843G>A , LRG_423t1:c.7843G>A	NP_004406.2:p.Glu2615Lys
XM_011514323.1:c.6514G>A	XP_011512625.1:p.Glu2172Lys
NM_001008844.2:c.6046G>A	NP_001008844.1:p.Glu2016Lys
NM_001319034.1:c.6514G>A	NP_001305963.1:p.Glu2172Lys
NM_004415.3:c.7843G>A	NP_004406.2:p.Glu2615Lys
NM_004415.4:c.7843G>A MANE Select	NP_004406.2:p.Glu2615Lys
NM_001008844.3:c.6046G>A	NP_001008844.1:p.Glu2016Lys
NM_001319034.2:c.6514G>A	NP_001305963.1:p.Glu2172Lys