Canonical Allele Identifier: CA1845639404
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648714C= , CM000671.2:g.34648714C= GRCh38
NC_000009.11:g.34648711C= , CM000671.1:g.34648711C= GRCh37
NC_000009.10:g.34638711C= NCBI36
NG_009029.1:g.7077C=
NG_028966.1:g.1530C=
NG_009029.2:g.7126C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*276-48C= ENSP00000509954.1:n.*276-48C=
ENST00000378842.8:c.688-48C= MANE Select ENSP00000368119.4:n.688-48C=
ENST00000378842.7:c.688-48C= ENSP00000368119.3:n.688-48C=
ENST00000450095.6:c.361-48C= ENSP00000401956.2:n.361-48C=
ENST00000473506.6:c.*276-48C= ENSP00000432839.2:n.*276-48C=
ENST00000473529.5:n.847-48C=
ENST00000487381.5:n.1330C=
ENST00000489643.6:n.720C=
ENST00000554085.5:c.*432-48C= ENSP00000450419.1:n.*432-48C=
ENST00000554550.5:c.*308-48C= ENSP00000451435.1:n.*308-48C=
ENST00000554638.5:n.1160-48C=
ENST00000555020.5:n.1101C=
ENST00000555086.5:n.692-48C=
ENST00000555754.1:n.33-48C=
ENST00000556244.1:c.675-48C=
ENST00000556278.1:c.432+258C= ENSP00000451792.1:n.432+258C=
ENST00000557706.5:n.1250-48C=
NM_000155.3:c.688-48C= NP_000146.2:n.688-48C=
NM_001258332.1:c.361-48C= NP_001245261.1:n.361-48C=
NM_000155.4:c.688-48C= MANE Select NP_000146.2:n.688-48C=
NM_001258332.2:c.361-48C= NP_001245261.1:n.361-48C=