Canonical Allele Identifier: CA1845639379
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648690C= , CM000671.2:g.34648690C= GRCh38
NC_000009.11:g.34648687C= , CM000671.1:g.34648687C= GRCh37
NC_000009.10:g.34638687C= NCBI36
NG_009029.1:g.7053C=
NG_028966.1:g.1506C=
NG_009029.2:g.7102C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*276-72C= ENSP00000509954.1:n.*276-72C=
ENST00000378842.8:c.688-72C= MANE Select ENSP00000368119.4:n.688-72C=
ENST00000378842.7:c.688-72C= ENSP00000368119.3:n.688-72C=
ENST00000450095.6:c.361-72C= ENSP00000401956.2:n.361-72C=
ENST00000473506.6:c.*276-72C= ENSP00000432839.2:n.*276-72C=
ENST00000473529.5:n.847-72C=
ENST00000487381.5:n.1306C=
ENST00000489643.6:n.696C=
ENST00000554085.5:c.*432-72C= ENSP00000450419.1:n.*432-72C=
ENST00000554550.5:c.*308-72C= ENSP00000451435.1:n.*308-72C=
ENST00000554638.5:n.1160-72C=
ENST00000555020.5:n.1077C=
ENST00000555086.5:n.692-72C=
ENST00000555754.1:n.33-72C=
ENST00000556244.1:c.675-72C=
ENST00000556278.1:c.432+234C= ENSP00000451792.1:n.432+234C=
ENST00000557706.5:n.1250-72C=
NM_000155.3:c.688-72C= NP_000146.2:n.688-72C=
NM_001258332.1:c.361-72C= NP_001245261.1:n.361-72C=
NM_000155.4:c.688-72C= MANE Select NP_000146.2:n.688-72C=
NM_001258332.2:c.361-72C= NP_001245261.1:n.361-72C=