Canonical Allele Identifier: CA11382257

Gene: HPS3

Linked Data

• ClinVar Variation Id: 1291638
• ClinVar RCV Id: RCV001713518
• dbSNP Id: rs11719052
• gnomAD v2: 3-148863584-A-G
• gnomAD v3: 3-149145797-A-G
• gnomAD v4: 3-149145797-A-G
• MyVariant Identifiers: chr3:g.148863584A>G (hg19) ; chr3:g.149145797A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149145797A>G , CM000665.2:g.149145797A>G	GRCh38
NC_000003.11:g.148863584A>G , CM000665.1:g.148863584A>G	GRCh37
NC_000003.10:g.150346274A>G	NCBI36
NG_009847.1:g.21214A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296051.7:c.1163+251A>G MANE Select	ENSP00000296051.2:n.1163+251A>G
ENST00000296051.6:c.1163+251A>G	ENSP00000296051.2:n.1163+251A>G
ENST00000460120.5:c.668+251A>G	ENSP00000418230.1:n.668+251A>G
ENST00000462030.5:n.1762+251A>G
ENST00000486530.1:n.1196+251A>G
NM_001308258.1:c.668+251A>G	NP_001295187.1:n.668+251A>G
NM_032383.3:c.1163+251A>G	NP_115759.2:n.1163+251A>G
NM_032383.4:c.1163+251A>G	NP_115759.2:n.1163+251A>G
XM_005247834.3:c.1163+251A>G	XP_005247891.1:n.1163+251A>G
XM_006713788.1:c.1163+251A>G	XP_006713851.1:n.1163+251A>G
XR_924201.1:n.1278+251A>G
XM_005247834.4:c.1163+251A>G	XP_005247891.1:n.1163+251A>G
XM_017007323.2:c.1163+251A>G	XP_016862812.1:n.1163+251A>G
XR_001740326.2:n.1263+251A>G
XR_001740327.2:n.1263+251A>G
XR_001740328.2:n.1263+251A>G
XR_924201.3:n.1263+251A>G
NM_001308258.2:c.668+251A>G	NP_001295187.1:n.668+251A>G
NM_032383.5:c.1163+251A>G MANE Select	NP_115759.2:n.1163+251A>G