Canonical Allele Identifier: CA356565201
Community Standard Title: NM_006424.3(SLC34A2):c.113-2A>G
Gene: SLC34A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25662703A>G , CM000666.2:g.25662703A>G GRCh38
NC_000004.11:g.25664325A>G , CM000666.1:g.25664325A>G GRCh37
NC_000004.10:g.25273423A>G NCBI36
NG_021185.1:g.11891A>G

Transcript Alleles

HGVS Amino-acid Change
NM_006424.3:c.113-2A>G MANE Select NP_006415.3:n.113-2A>G
ENST00000382051.8:c.113-2A>G MANE Select ENSP00000371483.3:n.113-2A>G
NM_001177998.1:c.113-5A>G NP_001171469.1:n.113-5A>G
NM_001177998.2:c.113-5A>G NP_001171469.2:n.113-5A>G
NM_001177999.1:c.113-5A>G NP_001171470.1:n.113-5A>G
NM_001177999.2:c.113-5A>G NP_001171470.2:n.113-5A>G
NM_006424.2:c.113-2A>G NP_006415.2:n.113-2A>G
ENST00000382051.7:c.113-2A>G ENSP00000371483.3:n.113-2A>G
ENST00000503434.5:c.113-5A>G ENSP00000423021.1:n.113-5A>G
ENST00000504570.5:c.113-5A>G ENSP00000425501.1:n.113-5A>G
ENST00000507530.1:c.113-2A>G ENSP00000424266.1:n.113-2A>G
ENST00000513204.5:c.113-5A>G ENSP00000423038.1:n.113-5A>G
ENST00000645788.1:c.113-5A>G ENSP00000494094.1:n.113-5A>G