Canonical Allele Identifier: CA1845640200
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648974C= , CM000671.2:g.34648974C= GRCh38
NC_000009.11:g.34648971C= , CM000671.1:g.34648971C= GRCh37
NC_000009.10:g.34638971C= NCBI36
NG_009029.1:g.7337C=
NG_028966.1:g.1790C=
NG_009029.2:g.7386C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*409-24C= ENSP00000509954.1:n.*409-24C=
ENST00000378842.8:c.821-24C= MANE Select ENSP00000368119.4:n.821-24C=
ENST00000378842.7:c.821-24C= ENSP00000368119.3:n.821-24C=
ENST00000450095.6:c.494-24C= ENSP00000401956.2:n.494-24C=
ENST00000488412.2:n.53C=
ENST00000489643.6:n.901-24C=
ENST00000554085.5:c.*565-24C= ENSP00000450419.1:n.*565-24C=
ENST00000554550.5:c.*441-24C= ENSP00000451435.1:n.*441-24C=
ENST00000554638.5:n.1293-24C=
ENST00000555020.5:n.1282-24C=
ENST00000555086.5:n.904C=
ENST00000555754.1:n.245C=
ENST00000556278.1:c.432+518C= ENSP00000451792.1:n.432+518C=
ENST00000557706.5:n.1396-24C=
NM_000155.3:c.821-24C= NP_000146.2:n.821-24C=
NM_001258332.1:c.494-24C= NP_001245261.1:n.494-24C=
NM_000155.4:c.821-24C= MANE Select NP_000146.2:n.821-24C=
NM_001258332.2:c.494-24C= NP_001245261.1:n.494-24C=