Canonical Allele Identifier: CA1845636572

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647690C= , CM000671.2:g.34647690C=	GRCh38
NC_000009.11:g.34647687C= , CM000671.1:g.34647687C=	GRCh37
NC_000009.10:g.34637687C=	NCBI36
NG_009029.1:g.6053C=
NG_028966.1:g.506C=
NG_009029.2:g.6102C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+123C=	ENSP00000509954.1:n.328+123C=
ENST00000378842.8:c.362C= MANE Select	ENSP00000368119.4:p.Ser121=
ENST00000378842.7:c.362C=	ENSP00000368119.3:p.Ser121=
ENST00000450095.6:c.51-142C=	ENSP00000401956.2:n.51-142C=
ENST00000465543.6:n.701C=
ENST00000472111.5:n.492C=
ENST00000473506.6:c.313C=	ENSP00000432839.2:p.Leu105=
ENST00000473529.5:n.498C=
ENST00000485531.1:n.677C=
ENST00000487381.5:n.621C=
ENST00000489643.6:n.283-425C=
ENST00000554085.5:c.*106C=	ENSP00000450419.1:n.*106C=
ENST00000554139.5:n.415C=
ENST00000554330.5:n.399C=
ENST00000554550.5:c.253-142C=	ENSP00000451435.1:n.253-142C=
ENST00000554638.5:n.708C=
ENST00000554897.5:c.253-142C=	ENSP00000450942.1:n.253-142C=
ENST00000554944.5:n.432C=
ENST00000555020.5:n.392C=
ENST00000555086.5:n.366C=
ENST00000555214.5:n.262-358C=
ENST00000556157.1:n.486C=
ENST00000556244.1:c.349C=
ENST00000556278.1:c.253-425C=	ENSP00000451792.1:n.253-425C=
ENST00000556403.5:n.464C=
ENST00000556494.5:n.483C=
ENST00000557541.5:n.506C=
ENST00000557706.5:n.798C=
NM_000155.3:c.362C=	NP_000146.2:p.Ser121=
NM_001258332.1:c.51-142C=	NP_001245261.1:n.51-142C=
NM_000155.4:c.362C= MANE Select	NP_000146.2:p.Ser121=
NM_001258332.2:c.51-142C=	NP_001245261.1:n.51-142C=