Canonical Allele Identifier: CA373278818

Gene: GALT

Linked Data

• gnomAD v4: 9-34647235-G-A
• MyVariant Identifiers: chr9:g.34647232G>A (hg19) ; chr9:g.34647235G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647235G>A , CM000671.2:g.34647235G>A	GRCh38
NC_000009.11:g.34647232G>A , CM000671.1:g.34647232G>A	GRCh37
NC_000009.10:g.34637232G>A	NCBI36
NG_009029.1:g.5598G>A
NG_028966.1:g.51G>A
NG_009029.2:g.5647G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.229G>A	ENSP00000509954.1:p.Gly77Arg
ENST00000378842.8:c.229G>A MANE Select	ENSP00000368119.4:p.Gly77Arg
ENST00000378842.7:c.229G>A	ENSP00000368119.3:p.Gly77Arg
ENST00000450095.6:c.27G>A	ENSP00000401956.2:p.Leu9=
ENST00000465543.6:n.568G>A
ENST00000468099.2:n.269G>A
ENST00000472111.5:n.270G>A
ENST00000473506.6:c.229G>A	ENSP00000432839.2:p.Gly77Arg
ENST00000473529.5:n.276G>A
ENST00000485531.1:n.222G>A
ENST00000487381.5:n.255G>A
ENST00000489643.6:n.259G>A
ENST00000554085.5:c.229G>A	ENSP00000450419.1:p.Gly77Arg
ENST00000554139.5:n.282G>A
ENST00000554330.5:n.226G>A
ENST00000554550.5:c.229G>A	ENSP00000451435.1:p.Gly77Arg
ENST00000554638.5:n.253G>A
ENST00000554897.5:c.229G>A	ENSP00000450942.1:p.Gly77Arg
ENST00000554944.5:n.259G>A
ENST00000555020.5:n.259G>A
ENST00000555086.5:n.233G>A
ENST00000555214.5:n.238G>A
ENST00000556157.1:n.336G>A
ENST00000556244.1:c.113G>A
ENST00000556278.1:c.229G>A	ENSP00000451792.1:p.Gly77Arg
ENST00000556403.5:n.242G>A
ENST00000556494.5:n.261G>A
ENST00000557541.5:n.422G>A
ENST00000557706.5:n.343G>A
NM_000155.3:c.229G>A	NP_000146.2:p.Gly77Arg
NM_001258332.1:c.27G>A	NP_001245261.1:p.Leu9=
NM_000155.4:c.229G>A MANE Select	NP_000146.2:p.Gly77Arg
NM_001258332.2:c.27G>A	NP_001245261.1:p.Leu9=