Canonical Allele Identifier: CA365322557
Gene: PDSS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107210503G>A , CM000668.2:g.107210503G>A GRCh38
NC_000006.11:g.107531707G>A , CM000668.1:g.107531707G>A GRCh37
NC_000006.10:g.107638400G>A NCBI36
NG_013033.1:g.254073C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369037.9:c.944C>T MANE Select ENSP00000358033.4:p.Ser315Leu
ENST00000369037.8:c.944C>T ENSP00000358033.4:p.Ser315Leu
ENST00000449027.1:c.119C>T ENSP00000392613.1:p.Ser40Leu
NM_020381.3:c.944C>T NP_065114.3:p.Ser315Leu
XM_011535956.1:c.944C>T XP_011534258.1:p.Ser315Leu
XM_011535957.1:c.876+1606C>T XP_011534259.1:n.876+1606C>T
XM_011535958.1:c.809C>T XP_011534260.1:p.Ser270Leu
XM_011535959.1:c.876+1606C>T XP_011534261.1:n.876+1606C>T
XM_011535960.1:c.536C>T XP_011534262.1:p.Ser179Leu
XM_011535961.1:c.703-16649C>T XP_011534263.1:n.703-16649C>T
XM_011535962.1:c.536C>T XP_011534264.1:p.Ser179Leu
XM_011535956.3:c.944C>T XP_011534258.1:p.Ser315Leu
XM_011535957.3:c.876+1606C>T XP_011534259.1:n.876+1606C>T
XM_011535958.3:c.809C>T XP_011534260.1:p.Ser270Leu
XM_011535959.3:c.876+1606C>T XP_011534261.1:n.876+1606C>T
XM_011535960.3:c.536C>T XP_011534262.1:p.Ser179Leu
XM_011535961.3:c.703-16649C>T XP_011534263.1:n.703-16649C>T
XM_011535962.2:c.536C>T XP_011534264.1:p.Ser179Leu
XM_017011082.2:c.944C>T XP_016866571.1:p.Ser315Leu
NM_020381.4:c.944C>T MANE Select NP_065114.3:p.Ser315Leu