Canonical Allele Identifier: CA2841301176
Gene: SLC34A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137236303del , CM000671.2:g.137236303del GRCh38
NC_000009.11:g.140130755del , CM000671.1:g.140130755del GRCh37
NC_000009.10:g.139250576del NCBI36
NG_017008.1:g.10547del
NG_017008.2:g.10403del

Transcript Alleles

HGVS Amino-acid Change
ENST00000673835.1:c.1687del MANE Select ENSP00000501114.1:p.Asp563ThrfsTer4
ENST00000361134.2:c.1687del ENSP00000355353.2:p.Asp563ThrfsTer4
ENST00000538474.5:c.1687del ENSP00000442397.1:p.Asp563ThrfsTer4
NM_001177316.1:c.1687del NP_001170787.1:p.Asp563ThrfsTer4
NM_001177317.1:c.1687del NP_001170788.1:p.Asp563ThrfsTer4
NM_080877.2:c.1687del NP_543153.1:p.Asp563ThrfsTer4
XM_017014292.1:c.1687del XP_016869781.1:p.Asp563ThrfsTer4
NM_001177316.2:c.1687del MANE Select NP_001170787.2:p.Asp563ThrfsTer4
NM_001177317.2:c.1687del NP_001170788.2:p.Asp563ThrfsTer4
NM_080877.3:c.1687del NP_543153.2:p.Asp563ThrfsTer4