Canonical Allele Identifier: CA151839944

Gene: PDE10A

Linked Data

• dbSNP Id: rs147954352
• gnomAD v2: 6-166128696-C-T
• gnomAD v3: 6-165715208-C-T
• gnomAD v4: 6-165715208-C-T
• MyVariant Identifiers: chr6:g.166128696C>T (hg19) ; chr6:g.165715208C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.165715208C>T , CM000668.2:g.165715208C>T	GRCh38
NC_000006.11:g.166128696C>T , CM000668.1:g.166128696C>T	GRCh37
NC_000006.10:g.166048686C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366882.7:c.-614-171640G>A	ENSP00000355847.3:n.-614-171640G>A
ENST00000685292.1:n.572-4055G>A
ENST00000647768.3:c.107-4055G>A	ENSP00000497930.3:n.107-4055G>A
ENST00000649882.1:n.551-4055G>A
ENST00000672859.1:c.-17-4055G>A	ENSP00000500900.1:n.-17-4055G>A
ENST00000672902.1:c.-17-4055G>A	ENSP00000500351.1:n.-17-4055G>A
ENST00000676766.1:c.107-171640G>A	ENSP00000504611.1:n.107-171640G>A
ENST00000678161.1:c.-17-4055G>A	ENSP00000503721.1:n.-17-4055G>A
ENST00000580695.1:n.497-171640G>A
XM_011535387.3:c.59-4055G>A	XP_011533689.2:n.59-4055G>A
XM_017010194.2:c.59-4055G>A	XP_016865683.1:n.59-4055G>A
XM_017010197.2:c.59-4055G>A	XP_016865686.1:n.59-4055G>A
XR_001743121.2:n.2134-4055G>A