Canonical Allele Identifier: CA1845636146
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647501C= , CM000671.2:g.34647501C= GRCh38
NC_000009.11:g.34647498C= , CM000671.1:g.34647498C= GRCh37
NC_000009.10:g.34637498C= NCBI36
NG_009029.1:g.5864C=
NG_028966.1:g.317C=
NG_009029.2:g.5913C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.262C= ENSP00000509954.1:p.Gln88=
ENST00000378842.8:c.262C= MANE Select ENSP00000368119.4:p.Gln88=
ENST00000378842.7:c.262C= ENSP00000368119.3:p.Gln88=
ENST00000450095.6:c.50+243C= ENSP00000401956.2:n.50+243C=
ENST00000465543.6:n.601C=
ENST00000468099.2:n.535C=
ENST00000472111.5:n.303C=
ENST00000473506.6:c.253-40C= ENSP00000432839.2:n.253-40C=
ENST00000473529.5:n.309C=
ENST00000485531.1:n.488C=
ENST00000487381.5:n.521C=
ENST00000489643.6:n.282+243C=
ENST00000554085.5:c.*6C= ENSP00000450419.1:n.*6C=
ENST00000554139.5:n.315C=
ENST00000554330.5:n.250-40C=
ENST00000554550.5:c.252+243C= ENSP00000451435.1:n.252+243C=
ENST00000554638.5:n.519C=
ENST00000554897.5:c.252+243C= ENSP00000450942.1:n.252+243C=
ENST00000554944.5:n.283-40C=
ENST00000555020.5:n.292C=
ENST00000555086.5:n.266C=
ENST00000555214.5:n.261+243C=
ENST00000556157.1:n.386C=
ENST00000556244.1:c.249C=
ENST00000556278.1:c.252+243C= ENSP00000451792.1:n.252+243C=
ENST00000556403.5:n.275C=
ENST00000556494.5:n.294C=
ENST00000557541.5:n.446-40C=
ENST00000557706.5:n.609C=
NM_000155.3:c.262C= NP_000146.2:p.Gln88=
NM_001258332.1:c.50+243C= NP_001245261.1:n.50+243C=
NM_000155.4:c.262C= MANE Select NP_000146.2:p.Gln88=
NM_001258332.2:c.50+243C= NP_001245261.1:n.50+243C=