Canonical Allele Identifier: CA464595861

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647694A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647697A>T , CM000671.2:g.34647697A>T	GRCh38
NC_000009.11:g.34647694A>T , CM000671.1:g.34647694A>T	GRCh37
NC_000009.10:g.34637694A>T	NCBI36
NG_009029.1:g.6060A>T
NG_028966.1:g.513A>T
NG_009029.2:g.6109A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+130A>T	ENSP00000509954.1:n.328+130A>T
ENST00000378842.8:c.369A>T MANE Select	ENSP00000368119.4:p.Arg123=
ENST00000378842.7:c.369A>T	ENSP00000368119.3:p.Arg123=
ENST00000450095.6:c.51-135A>T	ENSP00000401956.2:n.51-135A>T
ENST00000465543.6:n.708A>T
ENST00000472111.5:n.499A>T
ENST00000473506.6:c.320A>T	ENSP00000432839.2:p.Glu107Val
ENST00000473529.5:n.505A>T
ENST00000485531.1:n.684A>T
ENST00000487381.5:n.628A>T
ENST00000489643.6:n.283-418A>T
ENST00000554085.5:c.*113A>T	ENSP00000450419.1:n.*113A>T
ENST00000554139.5:n.422A>T
ENST00000554330.5:n.406A>T
ENST00000554550.5:c.253-135A>T	ENSP00000451435.1:n.253-135A>T
ENST00000554638.5:n.715A>T
ENST00000554897.5:c.253-135A>T	ENSP00000450942.1:n.253-135A>T
ENST00000554944.5:n.439A>T
ENST00000555020.5:n.399A>T
ENST00000555086.5:n.373A>T
ENST00000555214.5:n.262-351A>T
ENST00000556157.1:n.493A>T
ENST00000556244.1:c.356A>T
ENST00000556278.1:c.253-418A>T	ENSP00000451792.1:n.253-418A>T
ENST00000556403.5:n.471A>T
ENST00000556494.5:n.490A>T
ENST00000557541.5:n.513A>T
ENST00000557706.5:n.805A>T
NM_000155.3:c.369A>T	NP_000146.2:p.Arg123=
NM_001258332.1:c.51-135A>T	NP_001245261.1:n.51-135A>T
NM_000155.4:c.369A>T MANE Select	NP_000146.2:p.Arg123=
NM_001258332.2:c.51-135A>T	NP_001245261.1:n.51-135A>T