Canonical Allele Identifier: CA1410093900

Gene: HPS3

Linked Data

• dbSNP Id: rs1722742287

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149145575G>T , CM000665.2:g.149145575G>T	GRCh38
NC_000003.11:g.148863362G>T , CM000665.1:g.148863362G>T	GRCh37
NC_000003.10:g.150346052G>T	NCBI36
NG_009847.1:g.20992G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296051.7:c.1163+29G>T MANE Select	ENSP00000296051.2:n.1163+29G>T
ENST00000296051.6:c.1163+29G>T	ENSP00000296051.2:n.1163+29G>T
ENST00000460120.5:c.668+29G>T	ENSP00000418230.1:n.668+29G>T
ENST00000462030.5:n.1762+29G>T
ENST00000486530.1:n.1196+29G>T
NM_001308258.1:c.668+29G>T	NP_001295187.1:n.668+29G>T
NM_032383.3:c.1163+29G>T	NP_115759.2:n.1163+29G>T
NM_032383.4:c.1163+29G>T	NP_115759.2:n.1163+29G>T
XM_005247834.3:c.1163+29G>T	XP_005247891.1:n.1163+29G>T
XM_006713788.1:c.1163+29G>T	XP_006713851.1:n.1163+29G>T
XR_924201.1:n.1278+29G>T
XM_005247834.4:c.1163+29G>T	XP_005247891.1:n.1163+29G>T
XM_017007323.2:c.1163+29G>T	XP_016862812.1:n.1163+29G>T
XR_001740326.2:n.1263+29G>T
XR_001740327.2:n.1263+29G>T
XR_001740328.2:n.1263+29G>T
XR_924201.3:n.1263+29G>T
NM_001308258.2:c.668+29G>T	NP_001295187.1:n.668+29G>T
NM_032383.5:c.1163+29G>T MANE Select	NP_115759.2:n.1163+29G>T