Canonical Allele Identifier: CA552448946
Community Standard Title: NM_001098484.3(SLC4A4):c.2167-235_2167-234insG
Gene: SLC4A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71531827_71531828insG , CM000666.2:g.71531827_71531828insG GRCh38
NC_000004.11:g.72397544_72397545insG , CM000666.1:g.72397544_72397545insG GRCh37
NC_000004.10:g.72616408_72616409insG NCBI36
NG_012653.1:g.349542_349543insG

Transcript Alleles

HGVS Amino-acid Change
NM_001098484.3:c.2167-235_2167-234insG MANE Select NP_001091954.1:n.2167-235_2167-234insG
ENST00000264485.11:c.2167-235_2167-234insG MANE Select ENSP00000264485.5:n.2167-235_2167-234insG
NM_003759.4:c.2035-235_2035-234insG MANE Plus Clinical NP_003750.1:n.2035-235_2035-234insG
ENST00000340595.4:c.2035-235_2035-234insG MANE Plus Clinical ENSP00000344272.3:n.2035-235_2035-234insG
NM_001098484.2:c.2167-235_2167-234insG NP_001091954.1:n.2167-235_2167-234insG
NM_001134742.1:c.2167-235_2167-234insG NP_001128214.1:n.2167-235_2167-234insG
NM_001134742.2:c.2167-235_2167-234insG NP_001128214.1:n.2167-235_2167-234insG
NM_003759.3:c.2035-235_2035-234insG NP_003750.1:n.2035-235_2035-234insG
ENST00000264485.9:c.2167-235_2167-234insG ENSP00000264485.5:n.2167-235_2167-234insG
ENST00000340595.3:c.2035-235_2035-234insG ENSP00000344272.3:n.2035-235_2035-234insG
ENST00000351898.10:c.2167-235_2167-234insG ENSP00000307349.7:n.2167-235_2167-234insG
ENST00000425175.5:c.2167-235_2167-234insG ENSP00000393557.1:n.2167-235_2167-234insG
ENST00000649996.1:c.2167-235_2167-234insG ENSP00000497468.1:n.2167-235_2167-234insG
ENST00000698522.1:c.2263-235_2263-234insG ENSP00000513771.1:n.2263-235_2263-234insG
XM_011532390.1:c.1609-235_1609-234insG XP_011530692.1:n.1609-235_1609-234insG
XM_011532390.2:c.1609-235_1609-234insG XP_011530692.1:n.1609-235_1609-234insG
XM_017008792.1:c.1942-235_1942-234insG XP_016864281.1:n.1942-235_1942-234insG
XM_017008793.1:c.1651-235_1651-234insG XP_016864282.1:n.1651-235_1651-234insG
XM_024454267.1:c.2260-235_2260-234insG XP_024310035.1:n.2260-235_2260-234insG
XM_024454268.1:c.2182-235_2182-234insG XP_024310036.1:n.2182-235_2182-234insG
XM_024454269.1:c.2182-235_2182-234insG XP_024310037.1:n.2182-235_2182-234insG
XM_024454270.1:c.2167-235_2167-234insG XP_024310038.1:n.2167-235_2167-234insG
XM_024454271.1:c.2167-235_2167-234insG XP_024310039.1:n.2167-235_2167-234insG
XM_024454272.1:c.2167-235_2167-234insG XP_024310040.1:n.2167-235_2167-234insG