Canonical Allele Identifier: CA11747669
Gene: SLC34A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25657986T>C , CM000666.2:g.25657986T>C GRCh38
NC_000004.11:g.25659608T>C , CM000666.1:g.25659608T>C GRCh37
NC_000004.10:g.25268706T>C NCBI36
NG_021185.1:g.7174T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382051.8:c.-4+2096T>C MANE Select ENSP00000371483.3:n.-4+2096T>C
ENST00000645788.1:c.-3-4512T>C ENSP00000494094.1:n.-3-4512T>C
ENST00000382051.7:c.-4+2096T>C ENSP00000371483.3:n.-4+2096T>C
ENST00000503434.5:c.-4+1422T>C ENSP00000423021.1:n.-4+1422T>C
ENST00000504570.5:c.-4+2096T>C ENSP00000425501.1:n.-4+2096T>C
ENST00000507530.1:c.-4+1422T>C ENSP00000424266.1:n.-4+1422T>C
ENST00000513204.5:c.-4+2629T>C ENSP00000423038.1:n.-4+2629T>C
NM_001177998.1:c.-4+2096T>C NP_001171469.1:n.-4+2096T>C
NM_001177999.1:c.-4+1422T>C NP_001171470.1:n.-4+1422T>C
NM_006424.2:c.-4+2096T>C NP_006415.2:n.-4+2096T>C
NM_006424.3:c.-4+2096T>C MANE Select NP_006415.3:n.-4+2096T>C
NM_001177998.2:c.-4+2096T>C NP_001171469.2:n.-4+2096T>C
NM_001177999.2:c.-4+1422T>C NP_001171470.2:n.-4+1422T>C
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