Canonical Allele Identifier: CA339849285

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40557817C>G (hg19) ; chr1:g.40092145C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092145C>G , CM000663.2:g.40092145C>G	GRCh38
NC_000001.10:g.40557817C>G , CM000663.1:g.40557817C>G	GRCh37
NC_000001.9:g.40330404C>G	NCBI36
NG_009192.1:g.10326G>C , LRG_690:g.10326G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*98G>C	ENSP00000361865.5:n.*98G>C
ENST00000433473.8:c.259G>C	ENSP00000394863.4:p.Val87Leu
ENST00000439754.6:c.262G>C	ENSP00000403207.2:p.Val88Leu
ENST00000449045.7:c.125-2633G>C	ENSP00000392293.2:n.125-2633G>C
ENST00000526547.2:c.542G>C
ENST00000527311.7:c.234+253G>C	ENSP00000436695.3:n.234+253G>C
ENST00000530704.6:c.262G>C	ENSP00000431655.1:p.Val88Leu
ENST00000641083.1:c.240G>C
ENST00000641236.1:n.499G>C
ENST00000641319.1:c.262G>C	ENSP00000493128.1:p.Val88Leu
ENST00000641471.1:c.349G>C	ENSP00000493146.1:p.Val117Leu
ENST00000641548.1:c.*114G>C	ENSP00000492984.1:n.*114G>C
ENST00000641691.1:c.*114G>C	ENSP00000492910.1:n.*114G>C
ENST00000641924.1:c.124+4970G>C	ENSP00000493063.1:n.124+4970G>C
ENST00000642050.2:c.262G>C MANE Select	ENSP00000493153.1:p.Val88Leu
ENST00000372779.8:c.349G>C	ENSP00000361865.4:p.Val117Leu
ENST00000433473.7:c.262G>C	ENSP00000394863.3:p.Val88Leu
ENST00000449045.6:c.125-2633G>C	ENSP00000392293.2:n.125-2633G>C
ENST00000526547.1:c.112G>C	ENSP00000436481.1:p.Val38Leu
ENST00000527311.6:c.125-88G>C	ENSP00000436695.2:n.125-88G>C
ENST00000529905.5:c.262G>C	ENSP00000432053.1:p.Val88Leu
ENST00000530704.5:c.262G>C	ENSP00000431655.1:p.Val88Leu
NM_000310.3:c.262G>C , LRG_690t1:c.262G>C	NP_000301.1:p.Val88Leu
NM_001142604.1:c.125-2633G>C	NP_001136076.1:n.125-2633G>C
XM_005271008.1:c.262G>C	XP_005271065.1:p.Val88Leu
NM_001363695.1:c.262G>C	NP_001350624.1:p.Val88Leu
NM_000310.4:c.262G>C MANE Select	NP_000301.1:p.Val88Leu
NM_001142604.2:c.125-2633G>C	NP_001136076.1:n.125-2633G>C
NM_001363695.2:c.262G>C	NP_001350624.1:p.Val88Leu