Canonical Allele Identifier: CA365322670

Gene: PDSS2

Linked Data

• MyVariant Identifiers: chr6:g.107531757C>A (hg19) ; chr6:g.107210553C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107210553C>A , CM000668.2:g.107210553C>A	GRCh38
NC_000006.11:g.107531757C>A , CM000668.1:g.107531757C>A	GRCh37
NC_000006.10:g.107638450C>A	NCBI36
NG_013033.1:g.254023G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369037.9:c.894G>T MANE Select	ENSP00000358033.4:p.Gln298His
ENST00000369037.8:c.894G>T	ENSP00000358033.4:p.Gln298His
ENST00000449027.1:c.69G>T	ENSP00000392613.1:p.Gln23His
NM_020381.3:c.894G>T	NP_065114.3:p.Gln298His
XM_011535956.1:c.894G>T	XP_011534258.1:p.Gln298His
XM_011535957.1:c.876+1556G>T	XP_011534259.1:n.876+1556G>T
XM_011535958.1:c.759G>T	XP_011534260.1:p.Gln253His
XM_011535959.1:c.876+1556G>T	XP_011534261.1:n.876+1556G>T
XM_011535960.1:c.486G>T	XP_011534262.1:p.Gln162His
XM_011535961.1:c.703-16699G>T	XP_011534263.1:n.703-16699G>T
XM_011535962.1:c.486G>T	XP_011534264.1:p.Gln162His
XM_011535956.3:c.894G>T	XP_011534258.1:p.Gln298His
XM_011535957.3:c.876+1556G>T	XP_011534259.1:n.876+1556G>T
XM_011535958.3:c.759G>T	XP_011534260.1:p.Gln253His
XM_011535959.3:c.876+1556G>T	XP_011534261.1:n.876+1556G>T
XM_011535960.3:c.486G>T	XP_011534262.1:p.Gln162His
XM_011535961.3:c.703-16699G>T	XP_011534263.1:n.703-16699G>T
XM_011535962.2:c.486G>T	XP_011534264.1:p.Gln162His
XM_017011082.2:c.894G>T	XP_016866571.1:p.Gln298His
NM_020381.4:c.894G>T MANE Select	NP_065114.3:p.Gln298His