Canonical Allele Identifier: CA1845638706
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648371G= , CM000671.2:g.34648371G= GRCh38
NC_000009.11:g.34648368G= , CM000671.1:g.34648368G= GRCh37
NC_000009.10:g.34638368G= NCBI36
NG_009029.1:g.6734G=
NG_028966.1:g.1187G=
NG_009029.2:g.6783G=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*190G= ENSP00000509954.1:n.*190G=
ENST00000378842.8:c.602G= MANE Select ENSP00000368119.4:p.Arg201=
ENST00000378842.7:c.602G= ENSP00000368119.3:p.Arg201=
ENST00000450095.6:c.275G= ENSP00000401956.2:p.Arg92=
ENST00000472111.5:n.858G=
ENST00000473506.6:c.*190G= ENSP00000432839.2:n.*190G=
ENST00000473529.5:n.761G=
ENST00000485531.1:n.1196G=
ENST00000487381.5:n.987G=
ENST00000489643.6:n.377G=
ENST00000554085.5:c.*346G= ENSP00000450419.1:n.*346G=
ENST00000554139.5:n.848G=
ENST00000554550.5:c.*222G= ENSP00000451435.1:n.*222G=
ENST00000554638.5:n.1074G=
ENST00000554897.5:c.*289G= ENSP00000450942.1:n.*289G=
ENST00000554944.5:n.951G=
ENST00000555020.5:n.758G=
ENST00000555086.5:n.606G=
ENST00000555214.5:n.423G=
ENST00000556244.1:c.589G=
ENST00000556278.1:c.347G= ENSP00000451792.1:p.Arg116=
ENST00000556494.5:n.723G=
ENST00000557706.5:n.1164G=
NM_000155.3:c.602G= NP_000146.2:p.Arg201=
NM_001258332.1:c.275G= NP_001245261.1:p.Arg92=
NM_000155.4:c.602G= MANE Select NP_000146.2:p.Arg201=
NM_001258332.2:c.275G= NP_001245261.1:p.Arg92=