Canonical Allele Identifier: CA339849264

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40557813T>G (hg19) ; chr1:g.40092141T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092141T>G , CM000663.2:g.40092141T>G	GRCh38
NC_000001.10:g.40557813T>G , CM000663.1:g.40557813T>G	GRCh37
NC_000001.9:g.40330400T>G	NCBI36
NG_009192.1:g.10330A>C , LRG_690:g.10330A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*102A>C	ENSP00000361865.5:n.*102A>C
ENST00000433473.8:c.263A>C	ENSP00000394863.4:p.Asn88Thr
ENST00000439754.6:c.266A>C	ENSP00000403207.2:p.Asn89Thr
ENST00000449045.7:c.125-2629A>C	ENSP00000392293.2:n.125-2629A>C
ENST00000526547.2:c.546A>C
ENST00000527311.7:c.234+257A>C	ENSP00000436695.3:n.234+257A>C
ENST00000530704.6:c.266A>C	ENSP00000431655.1:p.Asn89Thr
ENST00000641083.1:c.244A>C
ENST00000641236.1:n.503A>C
ENST00000641319.1:c.266A>C	ENSP00000493128.1:p.Asn89Thr
ENST00000641471.1:c.353A>C	ENSP00000493146.1:p.Asn118Thr
ENST00000641548.1:c.*118A>C	ENSP00000492984.1:n.*118A>C
ENST00000641691.1:c.*118A>C	ENSP00000492910.1:n.*118A>C
ENST00000641924.1:c.124+4974A>C	ENSP00000493063.1:n.124+4974A>C
ENST00000642050.2:c.266A>C MANE Select	ENSP00000493153.1:p.Asn89Thr
ENST00000372779.8:c.353A>C	ENSP00000361865.4:p.Asn118Thr
ENST00000433473.7:c.266A>C	ENSP00000394863.3:p.Asn89Thr
ENST00000449045.6:c.125-2629A>C	ENSP00000392293.2:n.125-2629A>C
ENST00000526547.1:c.116A>C	ENSP00000436481.1:p.Asn39Thr
ENST00000527311.6:c.125-84A>C	ENSP00000436695.2:n.125-84A>C
ENST00000529905.5:c.266A>C	ENSP00000432053.1:p.Asn89Thr
ENST00000530704.5:c.266A>C	ENSP00000431655.1:p.Asn89Thr
NM_000310.3:c.266A>C , LRG_690t1:c.266A>C	NP_000301.1:p.Asn89Thr
NM_001142604.1:c.125-2629A>C	NP_001136076.1:n.125-2629A>C
XM_005271008.1:c.266A>C	XP_005271065.1:p.Asn89Thr
NM_001363695.1:c.266A>C	NP_001350624.1:p.Asn89Thr
NM_000310.4:c.266A>C MANE Select	NP_000301.1:p.Asn89Thr
NM_001142604.2:c.125-2629A>C	NP_001136076.1:n.125-2629A>C
NM_001363695.2:c.266A>C	NP_001350624.1:p.Asn89Thr