Canonical Allele Identifier: CA2566161659

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647620G>T , CM000671.2:g.34647620G>T	GRCh38
NC_000009.11:g.34647617G>T , CM000671.1:g.34647617G>T	GRCh37
NC_000009.10:g.34637617G>T	NCBI36
NG_009029.1:g.5983G>T
NG_028966.1:g.436G>T
NG_009029.2:g.6032G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.328+53G>T	ENSP00000509954.1:n.328+53G>T
ENST00000378842.8:c.329-37G>T MANE Select	ENSP00000368119.4:n.329-37G>T
ENST00000378842.7:c.329-37G>T	ENSP00000368119.3:n.329-37G>T
ENST00000450095.6:c.51-212G>T	ENSP00000401956.2:n.51-212G>T
ENST00000465543.6:n.668-37G>T
ENST00000472111.5:n.422G>T
ENST00000473506.6:c.280-37G>T	ENSP00000432839.2:n.280-37G>T
ENST00000473529.5:n.428G>T
ENST00000485531.1:n.607G>T
ENST00000487381.5:n.588-37G>T
ENST00000489643.6:n.282+362G>T
ENST00000554085.5:c.*73-37G>T	ENSP00000450419.1:n.*73-37G>T
ENST00000554139.5:n.382-37G>T
ENST00000554330.5:n.329G>T
ENST00000554550.5:c.253-212G>T	ENSP00000451435.1:n.253-212G>T
ENST00000554638.5:n.638G>T
ENST00000554897.5:c.253-212G>T	ENSP00000450942.1:n.253-212G>T
ENST00000554944.5:n.362G>T
ENST00000555020.5:n.359-37G>T
ENST00000555086.5:n.333-37G>T
ENST00000555214.5:n.261+362G>T
ENST00000556157.1:n.453-37G>T
ENST00000556244.1:c.316-37G>T
ENST00000556278.1:c.252+362G>T	ENSP00000451792.1:n.252+362G>T
ENST00000556403.5:n.394G>T
ENST00000556494.5:n.413G>T
ENST00000557541.5:n.473-37G>T
ENST00000557706.5:n.728G>T
NM_000155.3:c.329-37G>T	NP_000146.2:n.329-37G>T
NM_001258332.1:c.51-212G>T	NP_001245261.1:n.51-212G>T
NM_000155.4:c.329-37G>T MANE Select	NP_000146.2:n.329-37G>T
NM_001258332.2:c.51-212G>T	NP_001245261.1:n.51-212G>T