Canonical Allele Identifier: CA1845639924
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648864C= , CM000671.2:g.34648864C= GRCh38
NC_000009.11:g.34648861C= , CM000671.1:g.34648861C= GRCh37
NC_000009.10:g.34638861C= NCBI36
NG_009029.1:g.7227C=
NG_028966.1:g.1680C=
NG_009029.2:g.7276C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*378C= ENSP00000509954.1:n.*378C=
ENST00000378842.8:c.790C= MANE Select ENSP00000368119.4:p.Leu264=
ENST00000378842.7:c.790C= ENSP00000368119.3:p.Leu264=
ENST00000450095.6:c.463C= ENSP00000401956.2:p.Leu155=
ENST00000473506.6:c.*378C= ENSP00000432839.2:n.*378C=
ENST00000489643.6:n.870C=
ENST00000554085.5:c.*534C= ENSP00000450419.1:n.*534C=
ENST00000554550.5:c.*410C= ENSP00000451435.1:n.*410C=
ENST00000554638.5:n.1262C=
ENST00000555020.5:n.1251C=
ENST00000555086.5:n.794C=
ENST00000555754.1:n.135C=
ENST00000556244.1:c.777C=
ENST00000556278.1:c.432+408C= ENSP00000451792.1:n.432+408C=
ENST00000557706.5:n.1352C=
NM_000155.3:c.790C= NP_000146.2:p.Leu264=
NM_001258332.1:c.463C= NP_001245261.1:p.Leu155=
NM_000155.4:c.790C= MANE Select NP_000146.2:p.Leu264=
NM_001258332.2:c.463C= NP_001245261.1:p.Leu155=