Canonical Allele Identifier: CA1845639372
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648685C= , CM000671.2:g.34648685C= GRCh38
NC_000009.11:g.34648682C= , CM000671.1:g.34648682C= GRCh37
NC_000009.10:g.34638682C= NCBI36
NG_009029.1:g.7048C=
NG_028966.1:g.1501C=
NG_009029.2:g.7097C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.*276-77C= ENSP00000509954.1:n.*276-77C=
ENST00000378842.8:c.688-77C= MANE Select ENSP00000368119.4:n.688-77C=
ENST00000378842.7:c.688-77C= ENSP00000368119.3:n.688-77C=
ENST00000450095.6:c.361-77C= ENSP00000401956.2:n.361-77C=
ENST00000473506.6:c.*276-77C= ENSP00000432839.2:n.*276-77C=
ENST00000473529.5:n.847-77C=
ENST00000487381.5:n.1301C=
ENST00000489643.6:n.691C=
ENST00000554085.5:c.*432-77C= ENSP00000450419.1:n.*432-77C=
ENST00000554550.5:c.*308-77C= ENSP00000451435.1:n.*308-77C=
ENST00000554638.5:n.1160-77C=
ENST00000555020.5:n.1072C=
ENST00000555086.5:n.692-77C=
ENST00000555754.1:n.33-77C=
ENST00000556244.1:c.675-77C=
ENST00000556278.1:c.432+229C= ENSP00000451792.1:n.432+229C=
ENST00000557706.5:n.1250-77C=
NM_000155.3:c.688-77C= NP_000146.2:n.688-77C=
NM_001258332.1:c.361-77C= NP_001245261.1:n.361-77C=
NM_000155.4:c.688-77C= MANE Select NP_000146.2:n.688-77C=
NM_001258332.2:c.361-77C= NP_001245261.1:n.361-77C=