Canonical Allele Identifier: CA365322708

Gene: PDSS2

Linked Data

• MyVariant Identifiers: chr6:g.107531774T>A (hg19) ; chr6:g.107210570T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107210570T>A , CM000668.2:g.107210570T>A	GRCh38
NC_000006.11:g.107531774T>A , CM000668.1:g.107531774T>A	GRCh37
NC_000006.10:g.107638467T>A	NCBI36
NG_013033.1:g.254006A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369037.9:c.877A>T MANE Select	ENSP00000358033.4:p.Ile293Leu
ENST00000369037.8:c.877A>T	ENSP00000358033.4:p.Ile293Leu
ENST00000449027.1:c.52A>T	ENSP00000392613.1:p.Ile18Leu
NM_020381.3:c.877A>T	NP_065114.3:p.Ile293Leu
XM_011535956.1:c.877A>T	XP_011534258.1:p.Ile293Leu
XM_011535957.1:c.876+1539A>T	XP_011534259.1:n.876+1539A>T
XM_011535958.1:c.742A>T	XP_011534260.1:p.Ile248Leu
XM_011535959.1:c.876+1539A>T	XP_011534261.1:n.876+1539A>T
XM_011535960.1:c.469A>T	XP_011534262.1:p.Ile157Leu
XM_011535961.1:c.703-16716A>T	XP_011534263.1:n.703-16716A>T
XM_011535962.1:c.469A>T	XP_011534264.1:p.Ile157Leu
XM_011535956.3:c.877A>T	XP_011534258.1:p.Ile293Leu
XM_011535957.3:c.876+1539A>T	XP_011534259.1:n.876+1539A>T
XM_011535958.3:c.742A>T	XP_011534260.1:p.Ile248Leu
XM_011535959.3:c.876+1539A>T	XP_011534261.1:n.876+1539A>T
XM_011535960.3:c.469A>T	XP_011534262.1:p.Ile157Leu
XM_011535961.3:c.703-16716A>T	XP_011534263.1:n.703-16716A>T
XM_011535962.2:c.469A>T	XP_011534264.1:p.Ile157Leu
XM_017011082.2:c.877A>T	XP_016866571.1:p.Ile293Leu
NM_020381.4:c.877A>T MANE Select	NP_065114.3:p.Ile293Leu