Canonical Allele Identifier: CA1410093868

Gene: HPS3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149145498A= , CM000665.2:g.149145498A=	GRCh38
NC_000003.11:g.148863285A= , CM000665.1:g.148863285A=	GRCh37
NC_000003.10:g.150345975A=	NCBI36
NG_009847.1:g.20915A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296051.7:c.1115A= MANE Select	ENSP00000296051.2:p.Lys372=
ENST00000296051.6:c.1115A=	ENSP00000296051.2:p.Lys372=
ENST00000460120.5:c.620A=	ENSP00000418230.1:p.Lys207=
ENST00000462030.5:n.1714A=
ENST00000486530.1:n.1148A=
NM_001308258.1:c.620A=	NP_001295187.1:p.Lys207=
NM_032383.3:c.1115A=	NP_115759.2:p.Lys372=
NM_032383.4:c.1115A=	NP_115759.2:p.Lys372=
XM_005247834.3:c.1115A=	XP_005247891.1:p.Lys372=
XM_006713788.1:c.1115A=	XP_006713851.1:p.Lys372=
XR_924201.1:n.1230A=
XM_005247834.4:c.1115A=	XP_005247891.1:p.Lys372=
XM_017007323.2:c.1115A=	XP_016862812.1:p.Lys372=
XR_001740326.2:n.1215A=
XR_001740327.2:n.1215A=
XR_001740328.2:n.1215A=
XR_924201.3:n.1215A=
NM_001308258.2:c.620A=	NP_001295187.1:p.Lys207=
NM_032383.5:c.1115A= MANE Select	NP_115759.2:p.Lys372=