Canonical Allele Identifier: CA468482791

Gene: PDSS1

Linked Data

• MyVariant Identifiers: chr10:g.27012812T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26723883T>A , CM000672.2:g.26723883T>A	GRCh38
NC_000010.10:g.27012812T>A , CM000672.1:g.27012812T>A	GRCh37
NC_000010.9:g.27052818T>A	NCBI36
NG_008972.1:g.31218T>A
NG_008972.2:g.31218T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376215.10:c.687T>A MANE Select	ENSP00000365388.5:p.Ser229=
ENST00000376215.9:c.687T>A	ENSP00000365388.5:p.Ser229=
ENST00000473224.1:n.521T>A
ENST00000491711.5:c.95T>A
NM_014317.3:c.687T>A	NP_055132.2:p.Ser229=
XM_005252439.2:c.177T>A	XP_005252496.1:p.Ser59=
XM_011519437.1:c.318T>A	XP_011517739.1:p.Ser106=
XR_428636.2:n.975T>A
XR_930486.1:n.975T>A
NM_001321978.1:c.687T>A	NP_001308907.1:p.Ser229=
NM_001321979.1:c.177T>A	NP_001308908.1:p.Ser59=
NM_014317.4:c.687T>A	NP_055132.2:p.Ser229=
XM_011519437.3:c.318T>A	XP_011517739.1:p.Ser106=
XM_017016011.2:c.366T>A	XP_016871500.1:p.Ser122=
XM_024447922.1:c.687T>A	XP_024303690.1:p.Ser229=
XM_024447923.1:c.177T>A	XP_024303691.1:p.Ser59=
XR_428636.4:n.975T>A
NM_014317.5:c.687T>A MANE Select	NP_055132.2:p.Ser229=
NM_001321978.2:c.687T>A	NP_001308907.1:p.Ser229=
NM_001321979.2:c.177T>A	NP_001308908.1:p.Ser59=