Canonical Allele Identifier: CA1845637581

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647959C= , CM000671.2:g.34647959C=	GRCh38
NC_000009.11:g.34647956C= , CM000671.1:g.34647956C=	GRCh37
NC_000009.10:g.34637956C=	NCBI36
NG_009029.1:g.6322C=
NG_028966.1:g.775C=
NG_009029.2:g.6371C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*93C=	ENSP00000509954.1:n.*93C=
ENST00000378842.8:c.505C= MANE Select	ENSP00000368119.4:p.Gln169=
ENST00000378842.7:c.505C=	ENSP00000368119.3:p.Gln169=
ENST00000450095.6:c.178C=	ENSP00000401956.2:p.Gln60=
ENST00000465543.6:n.844C=
ENST00000472111.5:n.761C=
ENST00000473506.6:c.*93C=	ENSP00000432839.2:n.*93C=
ENST00000473529.5:n.641C=
ENST00000485531.1:n.946C=
ENST00000487381.5:n.890C=
ENST00000489643.6:n.283-156C=
ENST00000554085.5:c.*249C=	ENSP00000450419.1:n.*249C=
ENST00000554139.5:n.684C=
ENST00000554550.5:c.*125C=	ENSP00000451435.1:n.*125C=
ENST00000554638.5:n.977C=
ENST00000554897.5:c.*125C=	ENSP00000450942.1:n.*125C=
ENST00000554944.5:n.701C=
ENST00000555020.5:n.661C=
ENST00000555086.5:n.509C=
ENST00000555214.5:n.262-89C=
ENST00000556244.1:c.492C=
ENST00000556278.1:c.253-156C=	ENSP00000451792.1:n.253-156C=
ENST00000556494.5:n.626C=
ENST00000557706.5:n.1067C=
NM_000155.3:c.505C=	NP_000146.2:p.Gln169=
NM_001258332.1:c.178C=	NP_001245261.1:p.Gln60=
NM_000155.4:c.505C= MANE Select	NP_000146.2:p.Gln169=
NM_001258332.2:c.178C=	NP_001245261.1:p.Gln60=