Canonical Allele Identifier: CA376488847

Gene: PDSS1

Linked Data

• gnomAD v4: 10-26697749-C-G
• MyVariant Identifiers: chr10:g.26986678C>G (hg19) ; chr10:g.26697749C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26697749C>G , CM000672.2:g.26697749C>G	GRCh38
NC_000010.10:g.26986678C>G , CM000672.1:g.26986678C>G	GRCh37
NC_000010.9:g.27026684C>G	NCBI36
NG_008972.1:g.5084C>G
NG_008972.2:g.5084C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376215.10:c.38C>G MANE Select	ENSP00000365388.5:p.Ser13Cys
ENST00000376215.9:c.38C>G	ENSP00000365388.5:p.Ser13Cys
NM_014317.3:c.38C>G	NP_055132.2:p.Ser13Cys
XR_428636.2:n.326C>G
XR_930486.1:n.326C>G
NM_001321978.1:c.38C>G	NP_001308907.1:p.Ser13Cys
NM_001321979.1:c.-556C>G	NP_001308908.1:n.-556C>G
NM_014317.4:c.38C>G	NP_055132.2:p.Ser13Cys
XM_024447922.1:c.38C>G	XP_024303690.1:p.Ser13Cys
XR_428636.4:n.326C>G
NM_014317.5:c.38C>G MANE Select	NP_055132.2:p.Ser13Cys
NM_001321978.2:c.38C>G	NP_001308907.1:p.Ser13Cys
NM_001321979.2:c.-556C>G	NP_001308908.1:n.-556C>G