Canonical Allele Identifier: CA339847708

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40546106T>G (hg19) ; chr1:g.40080434T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40080434T>G , CM000663.2:g.40080434T>G	GRCh38
NC_000001.10:g.40546106T>G , CM000663.1:g.40546106T>G	GRCh37
NC_000001.9:g.40318693T>G	NCBI36
NG_009192.1:g.22037A>C , LRG_690:g.22037A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.587A>C	ENSP00000394863.4:p.Asn196Thr
ENST00000439754.6:c.590A>C	ENSP00000403207.2:p.Asn197Thr
ENST00000449045.7:c.281A>C	ENSP00000392293.2:p.Asn94Thr
ENST00000527311.7:c.359A>C	ENSP00000436695.3:p.Asn120Thr
ENST00000530076.6:c.-68A>C	ENSP00000434007.1:n.-68A>C
ENST00000530704.6:c.*213A>C	ENSP00000431655.1:n.*213A>C
ENST00000641083.1:c.568A>C
ENST00000641236.1:n.827A>C
ENST00000641319.1:c.590A>C	ENSP00000493128.1:p.Asn197Thr
ENST00000641381.1:c.149-3521A>C
ENST00000641471.1:c.677A>C	ENSP00000493146.1:p.Asn226Thr
ENST00000641691.1:c.*442A>C	ENSP00000492910.1:n.*442A>C
ENST00000641924.1:c.*19A>C	ENSP00000493063.1:n.*19A>C
ENST00000642050.2:c.590A>C MANE Select	ENSP00000493153.1:p.Asn197Thr
ENST00000372779.8:c.677A>C	ENSP00000361865.4:p.Asn226Thr
ENST00000433473.7:c.590A>C	ENSP00000394863.3:p.Asn197Thr
ENST00000439754.5:c.275A>C	ENSP00000403207.1:p.Asn92Thr
ENST00000449045.6:c.281A>C	ENSP00000392293.2:p.Asn94Thr
ENST00000527311.6:c.365A>C	ENSP00000436695.2:p.Asn122Thr
ENST00000529905.5:c.590A>C	ENSP00000432053.1:p.Asn197Thr
ENST00000530076.5:c.-68A>C	ENSP00000434007.1:n.-68A>C
ENST00000530704.5:c.*213A>C	ENSP00000431655.1:n.*213A>C
NM_000310.3:c.590A>C , LRG_690t1:c.590A>C	NP_000301.1:p.Asn197Thr
NM_001142604.1:c.281A>C	NP_001136076.1:p.Asn94Thr
XM_005271008.1:c.590A>C	XP_005271065.1:p.Asn197Thr
NM_001363695.1:c.590A>C	NP_001350624.1:p.Asn197Thr
NM_000310.4:c.590A>C MANE Select	NP_000301.1:p.Asn197Thr
NM_001142604.2:c.281A>C	NP_001136076.1:p.Asn94Thr
NM_001363695.2:c.590A>C	NP_001350624.1:p.Asn197Thr