Canonical Allele Identifier: CA1898170541

Gene: PDSS1

Linked Data

• dbSNP Id: rs1031182851

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26697898A>T , CM000672.2:g.26697898A>T	GRCh38
NC_000010.10:g.26986827A>T , CM000672.1:g.26986827A>T	GRCh37
NC_000010.9:g.27026833A>T	NCBI36
NG_008972.1:g.5233A>T
NG_008972.2:g.5233A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376215.10:c.129+58A>T MANE Select	ENSP00000365388.5:n.129+58A>T
ENST00000376215.9:c.129+58A>T	ENSP00000365388.5:n.129+58A>T
NM_014317.3:c.129+58A>T	NP_055132.2:n.129+58A>T
XR_428636.2:n.417+58A>T
XR_930486.1:n.417+58A>T
NM_001321978.1:c.129+58A>T	NP_001308907.1:n.129+58A>T
NM_001321979.1:c.-465+58A>T	NP_001308908.1:n.-465+58A>T
NM_014317.4:c.129+58A>T	NP_055132.2:n.129+58A>T
XM_024447922.1:c.129+58A>T	XP_024303690.1:n.129+58A>T
XR_428636.4:n.417+58A>T
NM_014317.5:c.129+58A>T MANE Select	NP_055132.2:n.129+58A>T
NM_001321978.2:c.129+58A>T	NP_001308907.1:n.129+58A>T
NM_001321979.2:c.-465+58A>T	NP_001308908.1:n.-465+58A>T