Canonical Allele Identifier: CA1845636409

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647631C= , CM000671.2:g.34647631C=	GRCh38
NC_000009.11:g.34647628C= , CM000671.1:g.34647628C=	GRCh37
NC_000009.10:g.34637628C=	NCBI36
NG_009029.1:g.5994C=
NG_028966.1:g.447C=
NG_009029.2:g.6043C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+64C=	ENSP00000509954.1:n.328+64C=
ENST00000378842.8:c.329-26C= MANE Select	ENSP00000368119.4:n.329-26C=
ENST00000378842.7:c.329-26C=	ENSP00000368119.3:n.329-26C=
ENST00000450095.6:c.51-201C=	ENSP00000401956.2:n.51-201C=
ENST00000465543.6:n.668-26C=
ENST00000472111.5:n.433C=
ENST00000473506.6:c.280-26C=	ENSP00000432839.2:n.280-26C=
ENST00000473529.5:n.439C=
ENST00000485531.1:n.618C=
ENST00000487381.5:n.588-26C=
ENST00000489643.6:n.282+373C=
ENST00000554085.5:c.*73-26C=	ENSP00000450419.1:n.*73-26C=
ENST00000554139.5:n.382-26C=
ENST00000554330.5:n.340C=
ENST00000554550.5:c.253-201C=	ENSP00000451435.1:n.253-201C=
ENST00000554638.5:n.649C=
ENST00000554897.5:c.253-201C=	ENSP00000450942.1:n.253-201C=
ENST00000554944.5:n.373C=
ENST00000555020.5:n.359-26C=
ENST00000555086.5:n.333-26C=
ENST00000555214.5:n.261+373C=
ENST00000556157.1:n.453-26C=
ENST00000556244.1:c.316-26C=
ENST00000556278.1:c.252+373C=	ENSP00000451792.1:n.252+373C=
ENST00000556403.5:n.405C=
ENST00000556494.5:n.424C=
ENST00000557541.5:n.473-26C=
ENST00000557706.5:n.739C=
NM_000155.3:c.329-26C=	NP_000146.2:n.329-26C=
NM_001258332.1:c.51-201C=	NP_001245261.1:n.51-201C=
NM_000155.4:c.329-26C= MANE Select	NP_000146.2:n.329-26C=
NM_001258332.2:c.51-201C=	NP_001245261.1:n.51-201C=