Canonical Allele Identifier: CA1898160386

Gene: PDSS1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26723844T= , CM000672.2:g.26723844T=	GRCh38
NC_000010.10:g.27012773T= , CM000672.1:g.27012773T=	GRCh37
NC_000010.9:g.27052779T=	NCBI36
NG_008972.1:g.31179T=
NG_008972.2:g.31179T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376215.10:c.648T= MANE Select	ENSP00000365388.5:p.Ser216=
ENST00000376215.9:c.648T=	ENSP00000365388.5:p.Ser216=
ENST00000473224.1:n.482T=
ENST00000491711.5:c.56T=
NM_014317.3:c.648T=	NP_055132.2:p.Ser216=
XM_005252439.2:c.138T=	XP_005252496.1:p.Ser46=
XM_011519437.1:c.279T=	XP_011517739.1:p.Ser93=
XR_428636.2:n.936T=
XR_930486.1:n.936T=
NM_001321978.1:c.648T=	NP_001308907.1:p.Ser216=
NM_001321979.1:c.138T=	NP_001308908.1:p.Ser46=
NM_014317.4:c.648T=	NP_055132.2:p.Ser216=
XM_011519437.3:c.279T=	XP_011517739.1:p.Ser93=
XM_017016011.2:c.327T=	XP_016871500.1:p.Ser109=
XM_024447922.1:c.648T=	XP_024303690.1:p.Ser216=
XM_024447923.1:c.138T=	XP_024303691.1:p.Ser46=
XR_428636.4:n.936T=
NM_014317.5:c.648T= MANE Select	NP_055132.2:p.Ser216=
NM_001321978.2:c.648T=	NP_001308907.1:p.Ser216=
NM_001321979.2:c.138T=	NP_001308908.1:p.Ser46=