Canonical Allele Identifier: CA1845640087
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648899G= , CM000671.2:g.34648899G= GRCh38
NC_000009.11:g.34648896G= , CM000671.1:g.34648896G= GRCh37
NC_000009.10:g.34638896G= NCBI36
NG_009029.1:g.7262G=
NG_028966.1:g.1715G=
NG_009029.2:g.7311G=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*408+5G= ENSP00000509954.1:n.*408+5G=
ENST00000378842.8:c.820+5G= MANE Select ENSP00000368119.4:n.820+5G=
ENST00000378842.7:c.820+5G= ENSP00000368119.3:n.820+5G=
ENST00000450095.6:c.493+5G= ENSP00000401956.2:n.493+5G=
ENST00000489643.6:n.900+5G=
ENST00000554085.5:c.*564+5G= ENSP00000450419.1:n.*564+5G=
ENST00000554550.5:c.*440+5G= ENSP00000451435.1:n.*440+5G=
ENST00000554638.5:n.1292+5G=
ENST00000555020.5:n.1281+5G=
ENST00000555086.5:n.829G=
ENST00000555754.1:n.170G=
ENST00000556278.1:c.432+443G= ENSP00000451792.1:n.432+443G=
ENST00000557706.5:n.1387G=
NM_000155.3:c.820+5G= NP_000146.2:n.820+5G=
NM_001258332.1:c.493+5G= NP_001245261.1:n.493+5G=
NM_000155.4:c.820+5G= MANE Select NP_000146.2:n.820+5G=
NM_001258332.2:c.493+5G= NP_001245261.1:n.493+5G=