Canonical Allele Identifier: CA1653773757

Gene: PDSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107245583C= , CM000668.2:g.107245583C=	GRCh38
NC_000006.11:g.107566787C= , CM000668.1:g.107566787C=	GRCh37
NC_000006.10:g.107673480C=	NCBI36
NG_013033.1:g.218993G=

Transcript Alleles

HGVS	Amino-acid Change
NM_020381.4:c.667G= MANE Select	NP_065114.3:p.Val223=
ENST00000369037.9:c.667G= MANE Select	ENSP00000358033.4:p.Val223=
NM_020381.3:c.667G=	NP_065114.3:p.Val223=
ENST00000369037.8:c.667G=	ENSP00000358033.4:p.Val223=
XM_011535956.1:c.667G=	XP_011534258.1:p.Val223=
XM_011535956.3:c.667G=	XP_011534258.1:p.Val223=
XM_011535957.1:c.667G=	XP_011534259.1:p.Val223=
XM_011535957.3:c.667G=	XP_011534259.1:p.Val223=
XM_011535958.1:c.532G=	XP_011534260.1:p.Val178=
XM_011535958.3:c.532G=	XP_011534260.1:p.Val178=
XM_011535959.1:c.667G=	XP_011534261.1:p.Val223=
XM_011535959.3:c.667G=	XP_011534261.1:p.Val223=
XM_011535960.1:c.259G=	XP_011534262.1:p.Val87=
XM_011535960.3:c.259G=	XP_011534262.1:p.Val87=
XM_011535961.1:c.667G=	XP_011534263.1:p.Val223=
XM_011535961.3:c.667G=	XP_011534263.1:p.Val223=
XM_011535962.1:c.259G=	XP_011534264.1:p.Val87=
XM_011535962.2:c.259G=	XP_011534264.1:p.Val87=
XM_017011082.2:c.667G=	XP_016866571.1:p.Val223=