Canonical Allele Identifier: CA1845636317

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647548G= , CM000671.2:g.34647548G=	GRCh38
NC_000009.11:g.34647545G= , CM000671.1:g.34647545G=	GRCh37
NC_000009.10:g.34637545G=	NCBI36
NG_009029.1:g.5911G=
NG_028966.1:g.364G=
NG_009029.2:g.5960G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.309G=	ENSP00000509954.1:p.Gln103=
ENST00000378842.8:c.309G= MANE Select	ENSP00000368119.4:p.Gln103=
ENST00000378842.7:c.309G=	ENSP00000368119.3:p.Gln103=
ENST00000450095.6:c.51-284G=	ENSP00000401956.2:n.51-284G=
ENST00000465543.6:n.648G=
ENST00000472111.5:n.350G=
ENST00000473506.6:c.260G=	ENSP00000432839.2:p.Ser87=
ENST00000473529.5:n.356G=
ENST00000485531.1:n.535G=
ENST00000487381.5:n.568G=
ENST00000489643.6:n.282+290G=
ENST00000554085.5:c.*53G=	ENSP00000450419.1:n.*53G=
ENST00000554139.5:n.362G=
ENST00000554330.5:n.257G=
ENST00000554550.5:c.253-284G=	ENSP00000451435.1:n.253-284G=
ENST00000554638.5:n.566G=
ENST00000554897.5:c.253-284G=	ENSP00000450942.1:n.253-284G=
ENST00000554944.5:n.290G=
ENST00000555020.5:n.339G=
ENST00000555086.5:n.313G=
ENST00000555214.5:n.261+290G=
ENST00000556157.1:n.433G=
ENST00000556244.1:c.296G=
ENST00000556278.1:c.252+290G=	ENSP00000451792.1:n.252+290G=
ENST00000556403.5:n.322G=
ENST00000556494.5:n.341G=
ENST00000557541.5:n.453G=
ENST00000557706.5:n.656G=
NM_000155.3:c.309G=	NP_000146.2:p.Gln103=
NM_001258332.1:c.51-284G=	NP_001245261.1:n.51-284G=
NM_000155.4:c.309G= MANE Select	NP_000146.2:p.Gln103=
NM_001258332.2:c.51-284G=	NP_001245261.1:n.51-284G=