Canonical Allele Identifier: CA1845638949
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648423A= , CM000671.2:g.34648423A= GRCh38
NC_000009.11:g.34648420A= , CM000671.1:g.34648420A= GRCh37
NC_000009.10:g.34638420A= NCBI36
NG_009029.1:g.6786A=
NG_028966.1:g.1239A=
NG_009029.2:g.6835A=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*242A= ENSP00000509954.1:n.*242A=
ENST00000378842.8:c.654A= MANE Select ENSP00000368119.4:p.Leu218=
ENST00000378842.7:c.654A= ENSP00000368119.3:p.Leu218=
ENST00000450095.6:c.327A= ENSP00000401956.2:p.Leu109=
ENST00000472111.5:n.910A=
ENST00000473506.6:c.*242A= ENSP00000432839.2:n.*242A=
ENST00000473529.5:n.813A=
ENST00000487381.5:n.1039A=
ENST00000489643.6:n.429A=
ENST00000554085.5:c.*398A= ENSP00000450419.1:n.*398A=
ENST00000554550.5:c.*274A= ENSP00000451435.1:n.*274A=
ENST00000554638.5:n.1126A=
ENST00000555020.5:n.810A=
ENST00000555086.5:n.658A=
ENST00000555214.5:n.475A=
ENST00000556244.1:c.641A=
ENST00000556278.1:c.399A= ENSP00000451792.1:p.Leu133=
ENST00000556494.5:n.775A=
ENST00000557706.5:n.1216A=
NM_000155.3:c.654A= NP_000146.2:p.Leu218=
NM_001258332.1:c.327A= NP_001245261.1:p.Leu109=
NM_000155.4:c.654A= MANE Select NP_000146.2:p.Leu218=
NM_001258332.2:c.327A= NP_001245261.1:p.Leu109=