Canonical Allele Identifier: CA1884372184

Gene: SLC34A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137236104_137236107delinsCCTG , CM000671.2:g.137236104_137236107delinsCCTG	GRCh38
NC_000009.11:g.140130556_140130559delinsCCTG , CM000671.1:g.140130556_140130559delinsCCTG	GRCh37
NC_000009.10:g.139250377_139250380delinsCCTG	NCBI36
NG_017008.1:g.10348_10351delinsCCTG
NG_017008.2:g.10204_10207delinsCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673835.1:c.1488_1491delinsCCTG MANE Select	ENSP00000501114.1:p.Phe496=
ENST00000361134.2:c.1488_1491delinsCCTG	ENSP00000355353.2:p.Phe496=
ENST00000538474.5:c.1488_1491delinsCCTG	ENSP00000442397.1:p.Phe496=
NM_001177316.1:c.1488_1491delinsCCTG	NP_001170787.1:p.Phe496=
NM_001177317.1:c.1488_1491delinsCCTG	NP_001170788.1:p.Phe496=
NM_080877.2:c.1488_1491delinsCCTG	NP_543153.1:p.Phe496=
XM_017014291.1:c.*47_*50delinsCCTG	XP_016869780.1:n.*47_*50delinsCCTG
XM_017014292.1:c.1488_1491delinsCCTG	XP_016869781.1:p.Phe496=
NM_001177316.2:c.1488_1491delinsCCTG MANE Select	NP_001170787.2:p.Phe496=
NM_001177317.2:c.1488_1491delinsCCTG	NP_001170788.2:p.Phe496=
NM_080877.3:c.1488_1491delinsCCTG	NP_543153.2:p.Phe496=