Canonical Allele Identifier: CA11314464
Gene: SLC4A5 HGNC NCBI

Linked Data

dbSNP Id: rs13006863
gnomAD v2: 2-74463566-C-T
gnomAD v3: 2-74236439-C-T
gnomAD v4: 2-74236439-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74236439C>T , CM000664.2:g.74236439C>T GRCh38
NC_000002.11:g.74463566C>T , CM000664.1:g.74463566C>T GRCh37
NC_000002.10:g.74317074C>T NCBI36
NG_032663.1:g.111969G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000394019.7:c.2320-1225G>A MANE Select ENSP00000377587.2:n.2320-1225G>A
ENST00000425249.6:c.2320-2876G>A ENSP00000405678.2:n.2320-2876G>A
ENST00000346834.8:c.2320-1225G>A ENSP00000251768.7:n.2320-1225G>A
ENST00000358683.8:c.2128-2876G>A ENSP00000351513.4:n.2128-2876G>A
ENST00000377632.5:c.2320-1225G>A ENSP00000366859.1:n.2320-1225G>A
ENST00000377634.8:c.2320-1225G>A ENSP00000366861.4:n.2320-1225G>A
ENST00000394019.6:c.2320-1225G>A ENSP00000377587.2:n.2320-1225G>A
ENST00000423644.5:c.2320-1225G>A ENSP00000395804.2:n.2320-1225G>A
ENST00000425249.5:c.2320-2876G>A ENSP00000405678.1:n.2320-2876G>A
ENST00000451608.2:c.3484-1225G>A ENSP00000416453.2:n.3484-1225G>A
ENST00000483195.5:n.3125-1225G>A
NM_021196.3:c.2320-1225G>A NP_067019.3:n.2320-1225G>A
NM_133478.2:c.2320-1225G>A NP_597812.1:n.2320-1225G>A
NM_133478.3:c.2320-1225G>A MANE Select NP_597812.1:n.2320-1225G>A
NM_001386136.1:c.1972-1225G>A NP_001373065.1:n.1972-1225G>A