Canonical Allele Identifier: CA365322522

Gene: PDSS2

Linked Data

• MyVariant Identifiers: chr6:g.107531689T>G (hg19) ; chr6:g.107210485T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107210485T>G , CM000668.2:g.107210485T>G	GRCh38
NC_000006.11:g.107531689T>G , CM000668.1:g.107531689T>G	GRCh37
NC_000006.10:g.107638382T>G	NCBI36
NG_013033.1:g.254091A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369037.9:c.962A>C MANE Select	ENSP00000358033.4:p.His321Pro
ENST00000369037.8:c.962A>C	ENSP00000358033.4:p.His321Pro
ENST00000449027.1:c.137A>C	ENSP00000392613.1:p.His46Pro
NM_020381.3:c.962A>C	NP_065114.3:p.His321Pro
XM_011535956.1:c.962A>C	XP_011534258.1:p.His321Pro
XM_011535957.1:c.876+1624A>C	XP_011534259.1:n.876+1624A>C
XM_011535958.1:c.827A>C	XP_011534260.1:p.His276Pro
XM_011535959.1:c.876+1624A>C	XP_011534261.1:n.876+1624A>C
XM_011535960.1:c.554A>C	XP_011534262.1:p.His185Pro
XM_011535961.1:c.703-16631A>C	XP_011534263.1:n.703-16631A>C
XM_011535962.1:c.554A>C	XP_011534264.1:p.His185Pro
XM_011535956.3:c.962A>C	XP_011534258.1:p.His321Pro
XM_011535957.3:c.876+1624A>C	XP_011534259.1:n.876+1624A>C
XM_011535958.3:c.827A>C	XP_011534260.1:p.His276Pro
XM_011535959.3:c.876+1624A>C	XP_011534261.1:n.876+1624A>C
XM_011535960.3:c.554A>C	XP_011534262.1:p.His185Pro
XM_011535961.3:c.703-16631A>C	XP_011534263.1:n.703-16631A>C
XM_011535962.2:c.554A>C	XP_011534264.1:p.His185Pro
XM_017011082.2:c.962A>C	XP_016866571.1:p.His321Pro
NM_020381.4:c.962A>C MANE Select	NP_065114.3:p.His321Pro