Canonical Allele Identifier: CA1845637071

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647851C= , CM000671.2:g.34647851C=	GRCh38
NC_000009.11:g.34647848C= , CM000671.1:g.34647848C=	GRCh37
NC_000009.10:g.34637848C=	NCBI36
NG_009029.1:g.6214C=
NG_028966.1:g.667C=
NG_009029.2:g.6263C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.348C=	ENSP00000509954.1:p.Thr116=
ENST00000378842.8:c.397C= MANE Select	ENSP00000368119.4:p.Pro133=
ENST00000378842.7:c.397C=	ENSP00000368119.3:p.Pro133=
ENST00000450095.6:c.70C=	ENSP00000401956.2:p.Pro24=
ENST00000465543.6:n.736C=
ENST00000472111.5:n.653C=
ENST00000473506.6:c.348C=	ENSP00000432839.2:p.Thr116=
ENST00000473529.5:n.533C=
ENST00000485531.1:n.838C=
ENST00000487381.5:n.782C=
ENST00000489643.6:n.283-264C=
ENST00000554085.5:c.*141C=	ENSP00000450419.1:n.*141C=
ENST00000554139.5:n.576C=
ENST00000554550.5:c.*17C=	ENSP00000451435.1:n.*17C=
ENST00000554638.5:n.869C=
ENST00000554897.5:c.*17C=	ENSP00000450942.1:n.*17C=
ENST00000554944.5:n.593C=
ENST00000555020.5:n.553C=
ENST00000555086.5:n.401C=
ENST00000555214.5:n.262-197C=
ENST00000556244.1:c.384C=
ENST00000556278.1:c.253-264C=	ENSP00000451792.1:n.253-264C=
ENST00000556494.5:n.518C=
ENST00000557541.5:n.541C=
ENST00000557706.5:n.959C=
NM_000155.3:c.397C=	NP_000146.2:p.Pro133=
NM_001258332.1:c.70C=	NP_001245261.1:p.Pro24=
NM_000155.4:c.397C= MANE Select	NP_000146.2:p.Pro133=
NM_001258332.2:c.70C=	NP_001245261.1:p.Pro24=