Canonical Allele Identifier: CA468624854

Gene: PDSS1

Linked Data

• gnomAD v4: 10-26697831-C-A
• MyVariant Identifiers: chr10:g.26986760C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26697831C>A , CM000672.2:g.26697831C>A	GRCh38
NC_000010.10:g.26986760C>A , CM000672.1:g.26986760C>A	GRCh37
NC_000010.9:g.27026766C>A	NCBI36
NG_008972.1:g.5166C>A
NG_008972.2:g.5166C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376215.10:c.120C>A MANE Select	ENSP00000365388.5:p.Val40=
ENST00000376215.9:c.120C>A	ENSP00000365388.5:p.Val40=
NM_014317.3:c.120C>A	NP_055132.2:p.Val40=
XR_428636.2:n.408C>A
XR_930486.1:n.408C>A
NM_001321978.1:c.120C>A	NP_001308907.1:p.Val40=
NM_001321979.1:c.-474C>A	NP_001308908.1:n.-474C>A
NM_014317.4:c.120C>A	NP_055132.2:p.Val40=
XM_024447922.1:c.120C>A	XP_024303690.1:p.Val40=
XR_428636.4:n.408C>A
NM_014317.5:c.120C>A MANE Select	NP_055132.2:p.Val40=
NM_001321978.2:c.120C>A	NP_001308907.1:p.Val40=
NM_001321979.2:c.-474C>A	NP_001308908.1:n.-474C>A