Canonical Allele Identifier: CA356569057
Community Standard Title: NM_006424.3(SLC34A2):c.1242G>T (p.Leu414Phe)
Gene: SLC34A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25674321G>T , CM000666.2:g.25674321G>T GRCh38
NC_000004.11:g.25675943G>T , CM000666.1:g.25675943G>T GRCh37
NC_000004.10:g.25285041G>T NCBI36
NG_021185.1:g.23509G>T

Transcript Alleles

HGVS Amino-acid Change
NM_006424.3:c.1242G>T MANE Select NP_006415.3:p.Leu414Phe
ENST00000382051.8:c.1242G>T MANE Select ENSP00000371483.3:p.Leu414Phe
NM_001177998.1:c.1239G>T NP_001171469.1:p.Leu413Phe
NM_001177998.2:c.1239G>T NP_001171469.2:p.Leu413Phe
NM_001177999.1:c.1239G>T NP_001171470.1:p.Leu413Phe
NM_001177999.2:c.1239G>T NP_001171470.2:p.Leu413Phe
NM_006424.2:c.1242G>T NP_006415.2:p.Leu414Phe
ENST00000382051.7:c.1242G>T ENSP00000371483.3:p.Leu414Phe
ENST00000503434.5:c.1239G>T ENSP00000423021.1:p.Leu413Phe
ENST00000504570.5:c.1239G>T ENSP00000425501.1:p.Leu413Phe
ENST00000645788.1:c.1239G>T ENSP00000494094.1:p.Leu413Phe