Canonical Allele Identifier: CA417322804

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40557803T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092131T>G , CM000663.2:g.40092131T>G	GRCh38
NC_000001.10:g.40557803T>G , CM000663.1:g.40557803T>G	GRCh37
NC_000001.9:g.40330390T>G	NCBI36
NG_009192.1:g.10340A>C , LRG_690:g.10340A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372779.9:c.*112A>C	ENSP00000361865.5:n.*112A>C
ENST00000433473.8:c.273A>C	ENSP00000394863.4:p.Val91=
ENST00000439754.6:c.276A>C	ENSP00000403207.2:p.Val92=
ENST00000449045.7:c.125-2619A>C	ENSP00000392293.2:n.125-2619A>C
ENST00000526547.2:c.556A>C
ENST00000527311.7:c.234+267A>C	ENSP00000436695.3:n.234+267A>C
ENST00000530704.6:c.276A>C	ENSP00000431655.1:p.Val92=
ENST00000641083.1:c.254A>C
ENST00000641236.1:n.513A>C
ENST00000641319.1:c.276A>C	ENSP00000493128.1:p.Val92=
ENST00000641471.1:c.363A>C	ENSP00000493146.1:p.Val121=
ENST00000641548.1:c.*128A>C	ENSP00000492984.1:n.*128A>C
ENST00000641691.1:c.*128A>C	ENSP00000492910.1:n.*128A>C
ENST00000641924.1:c.124+4984A>C	ENSP00000493063.1:n.124+4984A>C
ENST00000642050.2:c.276A>C MANE Select	ENSP00000493153.1:p.Val92=
ENST00000372779.8:c.363A>C	ENSP00000361865.4:p.Val121=
ENST00000433473.7:c.276A>C	ENSP00000394863.3:p.Val92=
ENST00000449045.6:c.125-2619A>C	ENSP00000392293.2:n.125-2619A>C
ENST00000526547.1:c.126A>C	ENSP00000436481.1:p.Val42=
ENST00000527311.6:c.125-74A>C	ENSP00000436695.2:n.125-74A>C
ENST00000529905.5:c.276A>C	ENSP00000432053.1:p.Val92=
ENST00000530704.5:c.276A>C	ENSP00000431655.1:p.Val92=
NM_000310.3:c.276A>C , LRG_690t1:c.276A>C	NP_000301.1:p.Val92=
NM_001142604.1:c.125-2619A>C	NP_001136076.1:n.125-2619A>C
XM_005271008.1:c.276A>C	XP_005271065.1:p.Val92=
NM_001363695.1:c.276A>C	NP_001350624.1:p.Val92=
NM_000310.4:c.276A>C MANE Select	NP_000301.1:p.Val92=
NM_001142604.2:c.125-2619A>C	NP_001136076.1:n.125-2619A>C
NM_001363695.2:c.276A>C	NP_001350624.1:p.Val92=