Canonical Allele Identifier: CA2608595038

Gene: PDSS1

Linked Data

• gnomAD v4: 10-26697919-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26697923dup , CM000672.2:g.26697923dup	GRCh38
NC_000010.10:g.26986852dup , CM000672.1:g.26986852dup	GRCh37
NC_000010.9:g.27026858dup	NCBI36
NG_008972.1:g.5258dup
NG_008972.2:g.5258dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376215.10:c.129+83dup MANE Select	ENSP00000365388.5:n.129+83dup
ENST00000376215.9:c.129+83dup	ENSP00000365388.5:n.129+83dup
NM_014317.3:c.129+83dup	NP_055132.2:n.129+83dup
XR_428636.2:n.417+83dup
XR_930486.1:n.417+83dup
NM_001321978.1:c.129+83dup	NP_001308907.1:n.129+83dup
NM_001321979.1:c.-465+83dup	NP_001308908.1:n.-465+83dup
NM_014317.4:c.129+83dup	NP_055132.2:n.129+83dup
XM_024447922.1:c.129+83dup	XP_024303690.1:n.129+83dup
XR_428636.4:n.417+83dup
NM_014317.5:c.129+83dup MANE Select	NP_055132.2:n.129+83dup
NM_001321978.2:c.129+83dup	NP_001308907.1:n.129+83dup
NM_001321979.2:c.-465+83dup	NP_001308908.1:n.-465+83dup