Canonical Allele Identifier: CA339847675

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40546100C>A (hg19) ; chr1:g.40080428C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40080428C>A , CM000663.2:g.40080428C>A	GRCh38
NC_000001.10:g.40546100C>A , CM000663.1:g.40546100C>A	GRCh37
NC_000001.9:g.40318687C>A	NCBI36
NG_009192.1:g.22043G>T , LRG_690:g.22043G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.593G>T	ENSP00000394863.4:p.Ser198Ile
ENST00000439754.6:c.596G>T	ENSP00000403207.2:p.Ser199Ile
ENST00000449045.7:c.287G>T	ENSP00000392293.2:p.Ser96Ile
ENST00000527311.7:c.365G>T	ENSP00000436695.3:p.Ser122Ile
ENST00000530076.6:c.-62G>T	ENSP00000434007.1:n.-62G>T
ENST00000530704.6:c.*219G>T	ENSP00000431655.1:n.*219G>T
ENST00000641083.1:c.574G>T
ENST00000641236.1:n.833G>T
ENST00000641319.1:c.596G>T	ENSP00000493128.1:p.Ser199Ile
ENST00000641381.1:c.149-3515G>T
ENST00000641471.1:c.683G>T	ENSP00000493146.1:p.Ser228Ile
ENST00000641691.1:c.*448G>T	ENSP00000492910.1:n.*448G>T
ENST00000641924.1:c.*25G>T	ENSP00000493063.1:n.*25G>T
ENST00000642050.2:c.596G>T MANE Select	ENSP00000493153.1:p.Ser199Ile
ENST00000372779.8:c.683G>T	ENSP00000361865.4:p.Ser228Ile
ENST00000433473.7:c.596G>T	ENSP00000394863.3:p.Ser199Ile
ENST00000439754.5:c.281G>T	ENSP00000403207.1:p.Ser94Ile
ENST00000449045.6:c.287G>T	ENSP00000392293.2:p.Ser96Ile
ENST00000527311.6:c.371G>T	ENSP00000436695.2:p.Ser124Ile
ENST00000529905.5:c.596G>T	ENSP00000432053.1:p.Ser199Ile
ENST00000530076.5:c.-62G>T	ENSP00000434007.1:n.-62G>T
ENST00000530704.5:c.*219G>T	ENSP00000431655.1:n.*219G>T
NM_000310.3:c.596G>T , LRG_690t1:c.596G>T	NP_000301.1:p.Ser199Ile
NM_001142604.1:c.287G>T	NP_001136076.1:p.Ser96Ile
XM_005271008.1:c.596G>T	XP_005271065.1:p.Ser199Ile
NM_001363695.1:c.596G>T	NP_001350624.1:p.Ser199Ile
NM_000310.4:c.596G>T MANE Select	NP_000301.1:p.Ser199Ile
NM_001142604.2:c.287G>T	NP_001136076.1:p.Ser96Ile
NM_001363695.2:c.596G>T	NP_001350624.1:p.Ser199Ile