Canonical Allele Identifier: CA1653746506

Gene: PDSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107154674G= , CM000668.2:g.107154674G=	GRCh38
NC_000006.11:g.107475878G= , CM000668.1:g.107475878G=	GRCh37
NC_000006.10:g.107582571G=	NCBI36
NG_013033.1:g.309902C=

Transcript Alleles

HGVS	Amino-acid Change
NM_020381.4:c.1145C= MANE Select	NP_065114.3:p.Ser382=
ENST00000369037.9:c.1145C= MANE Select	ENSP00000358033.4:p.Ser382=
NM_020381.3:c.1145C=	NP_065114.3:p.Ser382=
ENST00000369037.8:c.1145C=	ENSP00000358033.4:p.Ser382=
XM_011535956.1:c.1343C=	XP_011534258.1:p.Ser448=
XM_011535956.3:c.1343C=	XP_011534258.1:p.Ser448=
XM_011535957.1:c.1211C=	XP_011534259.1:p.Ser404=
XM_011535957.3:c.1211C=	XP_011534259.1:p.Ser404=
XM_011535958.1:c.1208C=	XP_011534260.1:p.Ser403=
XM_011535958.3:c.1208C=	XP_011534260.1:p.Ser403=
XM_011535959.1:c.1013C=	XP_011534261.1:p.Ser338=
XM_011535959.3:c.1013C=	XP_011534261.1:p.Ser338=
XM_011535960.1:c.935C=	XP_011534262.1:p.Ser312=
XM_011535960.3:c.935C=	XP_011534262.1:p.Ser312=
XM_011535961.1:c.839C=	XP_011534263.1:p.Ser280=
XM_011535961.3:c.839C=	XP_011534263.1:p.Ser280=
XM_011535962.1:c.737C=	XP_011534264.1:p.Ser246=
XM_011535962.2:c.737C=	XP_011534264.1:p.Ser246=