Canonical Allele Identifier: CA1845639845
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648851_34648852delinsGC , CM000671.2:g.34648851_34648852delinsGC GRCh38
NC_000009.11:g.34648848_34648849delinsGC , CM000671.1:g.34648848_34648849delinsGC GRCh37
NC_000009.10:g.34638848_34638849delinsGC NCBI36
NG_028966.1:g.1667_1668delinsGC
NG_009029.2:g.7263_7264delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.*365_*366delinsGC ENSP00000509954.1:n.*365_*366delinsGC
ENST00000378842.8:c.777_778delinsGC MANE Select ENSP00000368119.4:p.Arg259=
ENST00000378842.7:c.777_778delinsGC ENSP00000368119.3:p.Arg259=
ENST00000450095.6:c.450_451delinsGC ENSP00000401956.2:p.Arg150=
ENST00000473506.6:c.*365_*366delinsGC ENSP00000432839.2:n.*365_*366delinsGC
ENST00000489643.6:n.857_858delinsGC
ENST00000554085.5:c.*521_*522delinsGC ENSP00000450419.1:n.*521_*522delinsGC
ENST00000554550.5:c.*397_*398delinsGC ENSP00000451435.1:n.*397_*398delinsGC
ENST00000554638.5:n.1249_1250delinsGC
ENST00000555020.5:n.1238_1239delinsGC
ENST00000555086.5:n.781_782delinsGC
ENST00000555754.1:n.122_123delinsGC
ENST00000556244.1:c.764_765delinsGC
ENST00000556278.1:c.432+395_432+396delinsGC ENSP00000451792.1:n.432+395_432+396delinsGC
ENST00000557706.5:n.1339_1340delinsGC
NM_000155.3:c.777_778delinsGC NP_000146.2:p.Arg259=
NM_001258332.1:c.450_451delinsGC NP_001245261.1:p.Arg150=
NM_000155.4:c.777_778delinsGC MANE Select NP_000146.2:p.Arg259=
NM_001258332.2:c.450_451delinsGC NP_001245261.1:p.Arg150=