Canonical Allele Identifier: CA2506292839

Gene: PDSS1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26697953_26697959del , CM000672.2:g.26697953_26697959del	GRCh38
NC_000010.10:g.26986882_26986888del , CM000672.1:g.26986882_26986888del	GRCh37
NC_000010.9:g.27026888_27026894del	NCBI36
NG_008972.1:g.5288_5294del
NG_008972.2:g.5288_5294del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376215.10:c.129+113_129+119del MANE Select	ENSP00000365388.5:n.129+113_129+119del
ENST00000376215.9:c.129+113_129+119del	ENSP00000365388.5:n.129+113_129+119del
NM_014317.3:c.129+113_129+119del	NP_055132.2:n.129+113_129+119del
XR_428636.2:n.417+113_417+119del
XR_930486.1:n.417+113_417+119del
NM_001321978.1:c.129+113_129+119del	NP_001308907.1:n.129+113_129+119del
NM_001321979.1:c.-465+113_-465+119del	NP_001308908.1:n.-465+113_-465+119del
NM_014317.4:c.129+113_129+119del	NP_055132.2:n.129+113_129+119del
XM_024447922.1:c.129+113_129+119del	XP_024303690.1:n.129+113_129+119del
XR_428636.4:n.417+113_417+119del
NM_014317.5:c.129+113_129+119del MANE Select	NP_055132.2:n.129+113_129+119del
NM_001321978.2:c.129+113_129+119del	NP_001308907.1:n.129+113_129+119del
NM_001321979.2:c.-465+113_-465+119del	NP_001308908.1:n.-465+113_-465+119del