Canonical Allele Identifier: CA1898170558
Gene: PDSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.26697907A= , CM000672.2:g.26697907A= GRCh38
NC_000010.10:g.26986836A= , CM000672.1:g.26986836A= GRCh37
NC_000010.9:g.27026842A= NCBI36
NG_008972.1:g.5242A=
NG_008972.2:g.5242A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376215.10:c.129+67A= MANE Select ENSP00000365388.5:n.129+67A=
ENST00000376215.9:c.129+67A= ENSP00000365388.5:n.129+67A=
NM_014317.3:c.129+67A= NP_055132.2:n.129+67A=
XR_428636.2:n.417+67A=
XR_930486.1:n.417+67A=
NM_001321978.1:c.129+67A= NP_001308907.1:n.129+67A=
NM_001321979.1:c.-465+67A= NP_001308908.1:n.-465+67A=
NM_014317.4:c.129+67A= NP_055132.2:n.129+67A=
XM_024447922.1:c.129+67A= XP_024303690.1:n.129+67A=
XR_428636.4:n.417+67A=
NM_014317.5:c.129+67A= MANE Select NP_055132.2:n.129+67A=
NM_001321978.2:c.129+67A= NP_001308907.1:n.129+67A=
NM_001321979.2:c.-465+67A= NP_001308908.1:n.-465+67A=