Canonical Allele Identifier: CA436205987

Gene: HPS3

Linked Data

• MyVariant Identifiers: chr3:g.148863331A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149145544A>T , CM000665.2:g.149145544A>T	GRCh38
NC_000003.11:g.148863331A>T , CM000665.1:g.148863331A>T	GRCh37
NC_000003.10:g.150346021A>T	NCBI36
NG_009847.1:g.20961A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296051.7:c.1161A>T MANE Select	ENSP00000296051.2:p.Thr387=
ENST00000296051.6:c.1161A>T	ENSP00000296051.2:p.Thr387=
ENST00000460120.5:c.666A>T	ENSP00000418230.1:p.Thr222=
ENST00000462030.5:n.1760A>T
ENST00000486530.1:n.1194A>T
NM_001308258.1:c.666A>T	NP_001295187.1:p.Thr222=
NM_032383.3:c.1161A>T	NP_115759.2:p.Thr387=
NM_032383.4:c.1161A>T	NP_115759.2:p.Thr387=
XM_005247834.3:c.1161A>T	XP_005247891.1:p.Thr387=
XM_006713788.1:c.1161A>T	XP_006713851.1:p.Thr387=
XR_924201.1:n.1276A>T
XM_005247834.4:c.1161A>T	XP_005247891.1:p.Thr387=
XM_017007323.2:c.1161A>T	XP_016862812.1:p.Thr387=
XR_001740326.2:n.1261A>T
XR_001740327.2:n.1261A>T
XR_001740328.2:n.1261A>T
XR_924201.3:n.1261A>T
NM_001308258.2:c.666A>T	NP_001295187.1:p.Thr222=
NM_032383.5:c.1161A>T MANE Select	NP_115759.2:p.Thr387=