Canonical Allele Identifier: CA362694682

Gene: DSP

Linked Data

• ClinVar Variation Id: 1332503
• ClinVar RCV Id: RCV001805549 ; RCV002425081
• dbSNP Id: rs2113704486
• MyVariant Identifiers: chr6:g.7585708A>G (hg19) ; chr6:g.7585475A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585475A>G , CM000668.2:g.7585475A>G	GRCh38
NC_000006.11:g.7585708A>G , CM000668.1:g.7585708A>G	GRCh37
NC_000006.10:g.7530707A>G	NCBI36
NG_008803.1:g.48839A>G , LRG_423:g.48839A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6884A>G	ENSP00000518230.1:p.Asp2295Gly
ENST00000379802.8:c.8213A>G MANE Select	ENSP00000369129.3:p.Asp2738Gly
ENST00000379802.7:c.8213A>G	ENSP00000369129.3:p.Asp2738Gly
ENST00000418664.2:c.6416A>G	ENSP00000396591.2:p.Asp2139Gly
NM_001008844.1:c.6416A>G	NP_001008844.1:p.Asp2139Gly
NM_004415.2:c.8213A>G , LRG_423t1:c.8213A>G	NP_004406.2:p.Asp2738Gly
XM_011514323.1:c.6884A>G	XP_011512625.1:p.Asp2295Gly
NM_001008844.2:c.6416A>G	NP_001008844.1:p.Asp2139Gly
NM_001319034.1:c.6884A>G	NP_001305963.1:p.Asp2295Gly
NM_004415.3:c.8213A>G	NP_004406.2:p.Asp2738Gly
NM_004415.4:c.8213A>G MANE Select	NP_004406.2:p.Asp2738Gly
NM_001008844.3:c.6416A>G	NP_001008844.1:p.Asp2139Gly
NM_001319034.2:c.6884A>G	NP_001305963.1:p.Asp2295Gly