Canonical Allele Identifier: CA354921853

Gene: HPS3

Linked Data

• MyVariant Identifiers: chr3:g.148875251G>T (hg19) ; chr3:g.149157464G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149157464G>T , CM000665.2:g.149157464G>T	GRCh38
NC_000003.11:g.148875251G>T , CM000665.1:g.148875251G>T	GRCh37
NC_000003.10:g.150357941G>T	NCBI36
NG_009847.1:g.32881G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296051.7:c.1624G>T MANE Select	ENSP00000296051.2:p.Gly542Ter
ENST00000296051.6:c.1624G>T	ENSP00000296051.2:p.Gly542Ter
ENST00000460120.5:c.1129G>T	ENSP00000418230.1:p.Gly377Ter
NM_001308258.1:c.1129G>T	NP_001295187.1:p.Gly377Ter
NM_032383.3:c.1624G>T	NP_115759.2:p.Gly542Ter
NM_032383.4:c.1624G>T	NP_115759.2:p.Gly542Ter
XM_005247834.3:c.1624G>T	XP_005247891.1:p.Gly542Ter
XM_006713788.1:c.1624G>T	XP_006713851.1:p.Gly542Ter
XR_924201.1:n.1739G>T
XM_005247834.4:c.1624G>T	XP_005247891.1:p.Gly542Ter
XM_017007323.2:c.1624G>T	XP_016862812.1:p.Gly542Ter
XR_001740326.2:n.1724G>T
XR_001740327.2:n.1724G>T
XR_001740328.2:n.1724G>T
XR_924201.3:n.1724G>T
NM_001308258.2:c.1129G>T	NP_001295187.1:p.Gly377Ter
NM_032383.5:c.1624G>T MANE Select	NP_115759.2:p.Gly542Ter