Canonical Allele Identifier: CA1845639132
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648461G= , CM000671.2:g.34648461G= GRCh38
NC_000009.11:g.34648458G= , CM000671.1:g.34648458G= GRCh37
NC_000009.10:g.34638458G= NCBI36
NG_009029.1:g.6824G=
NG_028966.1:g.1277G=
NG_009029.2:g.6873G=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*275+5G= ENSP00000509954.1:n.*275+5G=
ENST00000378842.8:c.687+5G= MANE Select ENSP00000368119.4:n.687+5G=
ENST00000378842.7:c.687+5G= ENSP00000368119.3:n.687+5G=
ENST00000450095.6:c.360+5G= ENSP00000401956.2:n.360+5G=
ENST00000472111.5:n.948G=
ENST00000473506.6:c.*275+5G= ENSP00000432839.2:n.*275+5G=
ENST00000473529.5:n.846+5G=
ENST00000487381.5:n.1077G=
ENST00000489643.6:n.467G=
ENST00000554085.5:c.*431+5G= ENSP00000450419.1:n.*431+5G=
ENST00000554550.5:c.*307+5G= ENSP00000451435.1:n.*307+5G=
ENST00000554638.5:n.1159+5G=
ENST00000555020.5:n.848G=
ENST00000555086.5:n.691+5G=
ENST00000555214.5:n.513G=
ENST00000555754.1:n.32+5G=
ENST00000556244.1:c.674+5G=
ENST00000556278.1:c.432+5G= ENSP00000451792.1:n.432+5G=
ENST00000556494.5:n.813G=
ENST00000557706.5:n.1249+5G=
NM_000155.3:c.687+5G= NP_000146.2:n.687+5G=
NM_001258332.1:c.360+5G= NP_001245261.1:n.360+5G=
NM_000155.4:c.687+5G= MANE Select NP_000146.2:n.687+5G=
NM_001258332.2:c.360+5G= NP_001245261.1:n.360+5G=