Canonical Allele Identifier: CA2783504175
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647620dup , CM000671.2:g.34647620dup GRCh38
NC_000009.11:g.34647617dup , CM000671.1:g.34647617dup GRCh37
NC_000009.10:g.34637617dup NCBI36
NG_009029.1:g.5983dup
NG_028966.1:g.436dup
NG_009029.2:g.6032dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.328+53dup ENSP00000509954.1:n.328+53dup
ENST00000378842.8:c.329-37dup MANE Select ENSP00000368119.4:n.329-37dup
ENST00000378842.7:c.329-37dup ENSP00000368119.3:n.329-37dup
ENST00000450095.6:c.51-212dup ENSP00000401956.2:n.51-212dup
ENST00000465543.6:n.668-37dup
ENST00000472111.5:n.422dup
ENST00000473506.6:c.280-37dup ENSP00000432839.2:n.280-37dup
ENST00000473529.5:n.428dup
ENST00000485531.1:n.607dup
ENST00000487381.5:n.588-37dup
ENST00000489643.6:n.282+362dup
ENST00000554085.5:c.*73-37dup ENSP00000450419.1:n.*73-37dup
ENST00000554139.5:n.382-37dup
ENST00000554330.5:n.329dup
ENST00000554550.5:c.253-212dup ENSP00000451435.1:n.253-212dup
ENST00000554638.5:n.638dup
ENST00000554897.5:c.253-212dup ENSP00000450942.1:n.253-212dup
ENST00000554944.5:n.362dup
ENST00000555020.5:n.359-37dup
ENST00000555086.5:n.333-37dup
ENST00000555214.5:n.261+362dup
ENST00000556157.1:n.453-37dup
ENST00000556244.1:c.316-37dup
ENST00000556278.1:c.252+362dup ENSP00000451792.1:n.252+362dup
ENST00000556403.5:n.394dup
ENST00000556494.5:n.413dup
ENST00000557541.5:n.473-37dup
ENST00000557706.5:n.728dup
NM_000155.3:c.329-37dup NP_000146.2:n.329-37dup
NM_001258332.1:c.51-212dup NP_001245261.1:n.51-212dup
NM_000155.4:c.329-37dup MANE Select NP_000146.2:n.329-37dup
NM_001258332.2:c.51-212dup NP_001245261.1:n.51-212dup