Canonical Allele Identifier: CA1845636559
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647684_34647685delinsCA , CM000671.2:g.34647684_34647685delinsCA GRCh38
NC_000009.11:g.34647681_34647682delinsCA , CM000671.1:g.34647681_34647682delinsCA GRCh37
NC_000009.10:g.34637681_34637682delinsCA NCBI36
NG_009029.1:g.6047_6048delinsCA
NG_028966.1:g.500_501delinsCA
NG_009029.2:g.6096_6097delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.328+117_328+118delinsCA ENSP00000509954.1:n.328+117_328+118delinsCA
ENST00000378842.8:c.356_357delinsCA MANE Select ENSP00000368119.4:p.Ala119=
ENST00000378842.7:c.356_357delinsCA ENSP00000368119.3:p.Ala119=
ENST00000450095.6:c.51-148_51-147delinsCA ENSP00000401956.2:n.51-148_51-147delinsCA
ENST00000465543.6:n.695_696delinsCA
ENST00000472111.5:n.486_487delinsCA
ENST00000473506.6:c.307_308delinsCA ENSP00000432839.2:p.Gln103=
ENST00000473529.5:n.492_493delinsCA
ENST00000485531.1:n.671_672delinsCA
ENST00000487381.5:n.615_616delinsCA
ENST00000489643.6:n.282+426_282+427delinsCA
ENST00000554085.5:c.*100_*101delinsCA ENSP00000450419.1:n.*100_*101delinsCA
ENST00000554139.5:n.409_410delinsCA
ENST00000554330.5:n.393_394delinsCA
ENST00000554550.5:c.253-148_253-147delinsCA ENSP00000451435.1:n.253-148_253-147delinsCA
ENST00000554638.5:n.702_703delinsCA
ENST00000554897.5:c.253-148_253-147delinsCA ENSP00000450942.1:n.253-148_253-147delinsCA
ENST00000554944.5:n.426_427delinsCA
ENST00000555020.5:n.386_387delinsCA
ENST00000555086.5:n.360_361delinsCA
ENST00000555214.5:n.262-364_262-363delinsCA
ENST00000556157.1:n.480_481delinsCA
ENST00000556244.1:c.343_344delinsCA
ENST00000556278.1:c.252+426_252+427delinsCA ENSP00000451792.1:n.252+426_252+427delinsCA
ENST00000556403.5:n.458_459delinsCA
ENST00000556494.5:n.477_478delinsCA
ENST00000557541.5:n.500_501delinsCA
ENST00000557706.5:n.792_793delinsCA
NM_000155.3:c.356_357delinsCA NP_000146.2:p.Ala119=
NM_001258332.1:c.51-148_51-147delinsCA NP_001245261.1:n.51-148_51-147delinsCA
NM_000155.4:c.356_357delinsCA MANE Select NP_000146.2:p.Ala119=
NM_001258332.2:c.51-148_51-147delinsCA NP_001245261.1:n.51-148_51-147delinsCA