Canonical Allele Identifier: CA1603594258
Gene: SLC34A1 HGNC NCBI

Linked Data

dbSNP Id: rs6420094

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177390635A>C , CM000667.2:g.177390635A>C GRCh38
NC_000005.9:g.176817636A>C , CM000667.1:g.176817636A>C GRCh37
NC_000005.8:g.176750242A>C NCBI36
NG_016223.1:g.11205A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000324417.6:c.936+2263A>C MANE Select ENSP00000321424.4:n.936+2263A>C
ENST00000324417.5:c.936+2263A>C ENSP00000321424.4:n.936+2263A>C
ENST00000507685.5:n.1227+2263A>C
ENST00000513614.1:n.838+151A>C
NM_003052.4:c.936+2263A>C NP_003043.3:n.936+2263A>C
XM_005265975.1:c.936+2263A>C XP_005266032.1:n.936+2263A>C
XR_941112.1:n.1829+151A>C
XR_941113.1:n.1878A>C
XM_017009773.2:c.936+2263A>C XP_016865262.1:n.936+2263A>C
XM_017009774.1:c.-13+151A>C XP_016865263.1:n.-13+151A>C
XM_024446191.1:c.936+2263A>C XP_024301959.1:n.936+2263A>C
XR_941112.2:n.1883+151A>C
XR_941113.2:n.1932A>C
NM_003052.5:c.936+2263A>C MANE Select NP_003043.3:n.936+2263A>C