Canonical Allele Identifier: CA1845636357
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647582A= , CM000671.2:g.34647582A= GRCh38
NC_000009.11:g.34647579A= , CM000671.1:g.34647579A= GRCh37
NC_000009.10:g.34637579A= NCBI36
NG_009029.1:g.5945A=
NG_028966.1:g.398A=
NG_009029.2:g.5994A=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.328+15A= ENSP00000509954.1:n.328+15A=
ENST00000378842.8:c.328+15A= MANE Select ENSP00000368119.4:n.328+15A=
ENST00000378842.7:c.328+15A= ENSP00000368119.3:n.328+15A=
ENST00000450095.6:c.51-250A= ENSP00000401956.2:n.51-250A=
ENST00000465543.6:n.667+15A=
ENST00000472111.5:n.384A=
ENST00000473506.6:c.279+15A= ENSP00000432839.2:n.279+15A=
ENST00000473529.5:n.390A=
ENST00000485531.1:n.569A=
ENST00000487381.5:n.587+15A=
ENST00000489643.6:n.282+324A=
ENST00000554085.5:c.*72+15A= ENSP00000450419.1:n.*72+15A=
ENST00000554139.5:n.381+15A=
ENST00000554330.5:n.291A=
ENST00000554550.5:c.253-250A= ENSP00000451435.1:n.253-250A=
ENST00000554638.5:n.600A=
ENST00000554897.5:c.253-250A= ENSP00000450942.1:n.253-250A=
ENST00000554944.5:n.324A=
ENST00000555020.5:n.358+15A=
ENST00000555086.5:n.332+15A=
ENST00000555214.5:n.261+324A=
ENST00000556157.1:n.452+15A=
ENST00000556244.1:c.315+15A=
ENST00000556278.1:c.252+324A= ENSP00000451792.1:n.252+324A=
ENST00000556403.5:n.356A=
ENST00000556494.5:n.375A=
ENST00000557541.5:n.472+15A=
ENST00000557706.5:n.690A=
NM_000155.3:c.328+15A= NP_000146.2:n.328+15A=
NM_001258332.1:c.51-250A= NP_001245261.1:n.51-250A=
NM_000155.4:c.328+15A= MANE Select NP_000146.2:n.328+15A=
NM_001258332.2:c.51-250A= NP_001245261.1:n.51-250A=