Canonical Allele Identifier: CA118293
Gene: SLC4A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 6471
ClinVar RCV Id: RCV000006844
dbSNP Id: rs121908856

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71447706A>C , CM000666.2:g.71447706A>C GRCh38
NC_000004.11:g.72313423A>C , CM000666.1:g.72313423A>C GRCh37
NC_000004.10:g.72532287A>C NCBI36
NG_012653.1:g.265421A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698522.1:c.1122A>C ENSP00000513771.1:p.Arg374Ser
ENST00000264485.11:c.1026A>C MANE Select ENSP00000264485.5:p.Arg342Ser
ENST00000340595.4:c.894A>C MANE Plus Clinical ENSP00000344272.3:p.Arg298Ser
ENST00000649996.1:c.1026A>C ENSP00000497468.1:p.Arg342Ser
ENST00000264485.9:c.1026A>C ENSP00000264485.5:p.Arg342Ser
ENST00000340595.3:c.894A>C ENSP00000344272.3:p.Arg298Ser
ENST00000351898.10:c.1026A>C ENSP00000307349.7:p.Arg342Ser
ENST00000425175.5:c.1026A>C ENSP00000393557.1:p.Arg342Ser
ENST00000512686.5:c.894A>C ENSP00000422400.1:p.Arg298Ser
ENST00000514331.1:n.955A>C
NM_001098484.2:c.1026A>C NP_001091954.1:p.Arg342Ser
NM_001134742.1:c.1026A>C NP_001128214.1:p.Arg342Ser
NM_003759.3:c.894A>C NP_003750.1:p.Arg298Ser
XM_011532390.1:c.468A>C XP_011530692.1:p.Arg156Ser
XM_011532390.2:c.468A>C XP_011530692.1:p.Arg156Ser
XM_017008792.1:c.801A>C XP_016864281.1:p.Arg267Ser
XM_017008793.1:c.510A>C XP_016864282.1:p.Arg170Ser
XM_024454267.1:c.1119A>C XP_024310035.1:p.Arg373Ser
XM_024454268.1:c.1041A>C XP_024310036.1:p.Arg347Ser
XM_024454269.1:c.1041A>C XP_024310037.1:p.Arg347Ser
XM_024454270.1:c.1026A>C XP_024310038.1:p.Arg342Ser
XM_024454271.1:c.1026A>C XP_024310039.1:p.Arg342Ser
XM_024454272.1:c.1026A>C XP_024310040.1:p.Arg342Ser
NM_001098484.3:c.1026A>C MANE Select NP_001091954.1:p.Arg342Ser
NM_001134742.2:c.1026A>C NP_001128214.1:p.Arg342Ser
NM_003759.4:c.894A>C MANE Plus Clinical NP_003750.1:p.Arg298Ser