Canonical Allele Identifier: CA2721143217
Gene: PDSS1 HGNC NCBI

Linked Data

dbSNP Id: rs1241153547

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.26723773A>T , CM000672.2:g.26723773A>T GRCh38
NC_000010.10:g.27012702A>T , CM000672.1:g.27012702A>T GRCh37
NC_000010.9:g.27052708A>T NCBI36
NG_008972.1:g.31108A>T
NG_008972.2:g.31108A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376215.10:c.610-33A>T MANE Select ENSP00000365388.5:n.610-33A>T
ENST00000376215.9:c.610-33A>T ENSP00000365388.5:n.610-33A>T
ENST00000473224.1:n.444-33A>T
ENST00000491711.5:c.18-33A>T
NM_014317.3:c.610-33A>T NP_055132.2:n.610-33A>T
XM_005252439.2:c.100-33A>T XP_005252496.1:n.100-33A>T
XM_011519437.1:c.241-33A>T XP_011517739.1:n.241-33A>T
XR_428636.2:n.898-33A>T
XR_930486.1:n.898-33A>T
NM_001321978.1:c.610-33A>T NP_001308907.1:n.610-33A>T
NM_001321979.1:c.100-33A>T NP_001308908.1:n.100-33A>T
NM_014317.4:c.610-33A>T NP_055132.2:n.610-33A>T
XM_011519437.3:c.241-33A>T XP_011517739.1:n.241-33A>T
XM_017016011.2:c.289-33A>T XP_016871500.1:n.289-33A>T
XM_024447922.1:c.610-33A>T XP_024303690.1:n.610-33A>T
XM_024447923.1:c.100-33A>T XP_024303691.1:n.100-33A>T
XR_428636.4:n.898-33A>T
NM_014317.5:c.610-33A>T MANE Select NP_055132.2:n.610-33A>T
NM_001321978.2:c.610-33A>T NP_001308907.1:n.610-33A>T
NM_001321979.2:c.100-33A>T NP_001308908.1:n.100-33A>T