Canonical Allele Identifier: CA1845636361
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647589_34647590delinsCT , CM000671.2:g.34647589_34647590delinsCT GRCh38
NC_000009.11:g.34647586_34647587delinsCT , CM000671.1:g.34647586_34647587delinsCT GRCh37
NC_000009.10:g.34637586_34637587delinsCT NCBI36
NG_009029.1:g.5952_5953delinsCT
NG_028966.1:g.405_406delinsCT
NG_009029.2:g.6001_6002delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.328+22_328+23delinsCT ENSP00000509954.1:n.328+22_328+23delinsCT...
ENST00000378842.8:c.328+22_328+23delinsCT MANE Select ENSP00000368119.4:n.328+22_328+23delinsCT...
ENST00000378842.7:c.328+22_328+23delinsCT ENSP00000368119.3:n.328+22_328+23delinsCT...
ENST00000450095.6:c.51-243_51-242delinsCT ENSP00000401956.2:n.51-243_51-242delinsCT...
ENST00000465543.6:n.667+22_667+23delinsCT
ENST00000472111.5:n.391_392delinsCT
ENST00000473506.6:c.279+22_279+23delinsCT ENSP00000432839.2:n.279+22_279+23delinsCT...
ENST00000473529.5:n.397_398delinsCT
ENST00000485531.1:n.576_577delinsCT
ENST00000487381.5:n.587+22_587+23delinsCT
ENST00000489643.6:n.282+331_282+332delinsCT
ENST00000554085.5:c.*72+22_*72+23delinsCT ENSP00000450419.1:n.*72+22_*72+23delinsCT...
ENST00000554139.5:n.381+22_381+23delinsCT
ENST00000554330.5:n.298_299delinsCT
ENST00000554550.5:c.253-243_253-242delinsCT ENSP00000451435.1:n.253-243_253-242delins...
ENST00000554638.5:n.607_608delinsCT
ENST00000554897.5:c.253-243_253-242delinsCT ENSP00000450942.1:n.253-243_253-242delins...
ENST00000554944.5:n.331_332delinsCT
ENST00000555020.5:n.358+22_358+23delinsCT
ENST00000555086.5:n.332+22_332+23delinsCT
ENST00000555214.5:n.261+331_261+332delinsCT
ENST00000556157.1:n.452+22_452+23delinsCT
ENST00000556244.1:c.315+22_315+23delinsCT
ENST00000556278.1:c.252+331_252+332delinsCT ENSP00000451792.1:n.252+331_252+332delins...
ENST00000556403.5:n.363_364delinsCT
ENST00000556494.5:n.382_383delinsCT
ENST00000557541.5:n.472+22_472+23delinsCT
ENST00000557706.5:n.697_698delinsCT
NM_000155.3:c.328+22_328+23delinsCT NP_000146.2:n.328+22_328+23delinsCT
NM_001258332.1:c.51-243_51-242delinsCT NP_001245261.1:n.51-243_51-242delinsCT
NM_000155.4:c.328+22_328+23delinsCT MANE Select NP_000146.2:n.328+22_328+23delinsCT
NM_001258332.2:c.51-243_51-242delinsCT NP_001245261.1:n.51-243_51-242delinsCT