Canonical Allele Identifier: CA1653773801

Gene: PDSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107245646_107245649delinsTAAA , CM000668.2:g.107245646_107245649delinsTAAA	GRCh38
NC_000006.11:g.107566850_107566853delinsTAAA , CM000668.1:g.107566850_107566853delinsTAAA	GRCh37
NC_000006.10:g.107673543_107673546delinsTAAA	NCBI36
NG_013033.1:g.218927_218930delinsTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369037.9:c.631-30_631-27delinsTTTA MANE Select	ENSP00000358033.4:n.631-30_631-27delinsTTTA
ENST00000369037.8:c.631-30_631-27delinsTTTA	ENSP00000358033.4:n.631-30_631-27delinsTTTA
NM_020381.3:c.631-30_631-27delinsTTTA	NP_065114.3:n.631-30_631-27delinsTTTA
XM_011535956.1:c.631-30_631-27delinsTTTA	XP_011534258.1:n.631-30_631-27delinsTTTA
XM_011535957.1:c.631-30_631-27delinsTTTA	XP_011534259.1:n.631-30_631-27delinsTTTA
XM_011535958.1:c.496-30_496-27delinsTTTA	XP_011534260.1:n.496-30_496-27delinsTTTA
XM_011535959.1:c.631-30_631-27delinsTTTA	XP_011534261.1:n.631-30_631-27delinsTTTA
XM_011535960.1:c.223-30_223-27delinsTTTA	XP_011534262.1:n.223-30_223-27delinsTTTA
XM_011535961.1:c.631-30_631-27delinsTTTA	XP_011534263.1:n.631-30_631-27delinsTTTA
XM_011535962.1:c.223-30_223-27delinsTTTA	XP_011534264.1:n.223-30_223-27delinsTTTA
XM_011535956.3:c.631-30_631-27delinsTTTA	XP_011534258.1:n.631-30_631-27delinsTTTA
XM_011535957.3:c.631-30_631-27delinsTTTA	XP_011534259.1:n.631-30_631-27delinsTTTA
XM_011535958.3:c.496-30_496-27delinsTTTA	XP_011534260.1:n.496-30_496-27delinsTTTA
XM_011535959.3:c.631-30_631-27delinsTTTA	XP_011534261.1:n.631-30_631-27delinsTTTA
XM_011535960.3:c.223-30_223-27delinsTTTA	XP_011534262.1:n.223-30_223-27delinsTTTA
XM_011535961.3:c.631-30_631-27delinsTTTA	XP_011534263.1:n.631-30_631-27delinsTTTA
XM_011535962.2:c.223-30_223-27delinsTTTA	XP_011534264.1:n.223-30_223-27delinsTTTA
XM_017011082.2:c.631-30_631-27delinsTTTA	XP_016866571.1:n.631-30_631-27delinsTTTA
NM_020381.4:c.631-30_631-27delinsTTTA MANE Select	NP_065114.3:n.631-30_631-27delinsTTTA