Canonical Allele Identifier: CA1898170156
Gene: PDSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.26697752G= , CM000672.2:g.26697752G= GRCh38
NC_000010.10:g.26986681G= , CM000672.1:g.26986681G= GRCh37
NC_000010.9:g.27026687G= NCBI36
NG_008972.1:g.5087G=
NG_008972.2:g.5087G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376215.10:c.41G= MANE Select ENSP00000365388.5:p.Trp14=
ENST00000376215.9:c.41G= ENSP00000365388.5:p.Trp14=
NM_014317.3:c.41G= NP_055132.2:p.Trp14=
XR_428636.2:n.329G=
XR_930486.1:n.329G=
NM_001321978.1:c.41G= NP_001308907.1:p.Trp14=
NM_001321979.1:c.-553G= NP_001308908.1:n.-553G=
NM_014317.4:c.41G= NP_055132.2:p.Trp14=
XM_024447922.1:c.41G= XP_024303690.1:p.Trp14=
XR_428636.4:n.329G=
NM_014317.5:c.41G= MANE Select NP_055132.2:p.Trp14=
NM_001321978.2:c.41G= NP_001308907.1:p.Trp14=
NM_001321979.2:c.-553G= NP_001308908.1:n.-553G=