Canonical Allele Identifier: CA2668134951

Gene: HPS3

Linked Data

• gnomAD v4: 3-149157581-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149157581G>T , CM000665.2:g.149157581G>T	GRCh38
NC_000003.11:g.148875368G>T , CM000665.1:g.148875368G>T	GRCh37
NC_000003.10:g.150358058G>T	NCBI36
NG_009847.1:g.32998G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296051.7:c.1691+50G>T MANE Select	ENSP00000296051.2:n.1691+50G>T
ENST00000296051.6:c.1691+50G>T	ENSP00000296051.2:n.1691+50G>T
ENST00000460120.5:c.1196+50G>T	ENSP00000418230.1:n.1196+50G>T
NM_001308258.1:c.1196+50G>T	NP_001295187.1:n.1196+50G>T
NM_032383.3:c.1691+50G>T	NP_115759.2:n.1691+50G>T
NM_032383.4:c.1691+50G>T	NP_115759.2:n.1691+50G>T
XM_005247834.3:c.1691+50G>T	XP_005247891.1:n.1691+50G>T
XM_006713788.1:c.1691+50G>T	XP_006713851.1:n.1691+50G>T
XR_924201.1:n.1806+50G>T
XM_005247834.4:c.1691+50G>T	XP_005247891.1:n.1691+50G>T
XM_017007323.2:c.1691+50G>T	XP_016862812.1:n.1691+50G>T
XR_001740326.2:n.1791+50G>T
XR_001740327.2:n.1791+50G>T
XR_001740328.2:n.1791+50G>T
XR_924201.3:n.1791+50G>T
NM_001308258.2:c.1196+50G>T	NP_001295187.1:n.1196+50G>T
NM_032383.5:c.1691+50G>T MANE Select	NP_115759.2:n.1691+50G>T