Canonical Allele Identifier: CA151839942

Gene: PDE10A

Linked Data

• dbSNP Id: rs764104647
• gnomAD v3: 6-165715201-A-G
• gnomAD v4: 6-165715201-A-G
• MyVariant Identifiers: chr6:g.166128689A>G (hg19) ; chr6:g.165715201A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.165715201A>G , CM000668.2:g.165715201A>G	GRCh38
NC_000006.11:g.166128689A>G , CM000668.1:g.166128689A>G	GRCh37
NC_000006.10:g.166048679A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366882.7:c.-614-171633T>C	ENSP00000355847.3:n.-614-171633T>C
ENST00000685292.1:n.572-4048T>C
ENST00000647768.3:c.107-4048T>C	ENSP00000497930.3:n.107-4048T>C
ENST00000649882.1:n.551-4048T>C
ENST00000672859.1:c.-17-4048T>C	ENSP00000500900.1:n.-17-4048T>C
ENST00000672902.1:c.-17-4048T>C	ENSP00000500351.1:n.-17-4048T>C
ENST00000676766.1:c.107-171633T>C	ENSP00000504611.1:n.107-171633T>C
ENST00000678161.1:c.-17-4048T>C	ENSP00000503721.1:n.-17-4048T>C
ENST00000580695.1:n.497-171633T>C
XM_011535387.3:c.59-4048T>C	XP_011533689.2:n.59-4048T>C
XM_017010194.2:c.59-4048T>C	XP_016865683.1:n.59-4048T>C
XM_017010197.2:c.59-4048T>C	XP_016865686.1:n.59-4048T>C
XR_001743121.2:n.2134-4048T>C