Canonical Allele Identifier: CA464595820

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647670C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647673C>G , CM000671.2:g.34647673C>G	GRCh38
NC_000009.11:g.34647670C>G , CM000671.1:g.34647670C>G	GRCh37
NC_000009.10:g.34637670C>G	NCBI36
NG_009029.1:g.6036C>G
NG_028966.1:g.489C>G
NG_009029.2:g.6085C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.328+106C>G	ENSP00000509954.1:n.328+106C>G
ENST00000378842.8:c.345C>G MANE Select	ENSP00000368119.4:p.Pro115=
ENST00000378842.7:c.345C>G	ENSP00000368119.3:p.Pro115=
ENST00000450095.6:c.51-159C>G	ENSP00000401956.2:n.51-159C>G
ENST00000465543.6:n.684C>G
ENST00000472111.5:n.475C>G
ENST00000473506.6:c.296C>G	ENSP00000432839.2:p.Pro99Arg
ENST00000473529.5:n.481C>G
ENST00000485531.1:n.660C>G
ENST00000487381.5:n.604C>G
ENST00000489643.6:n.282+415C>G
ENST00000554085.5:c.*89C>G	ENSP00000450419.1:n.*89C>G
ENST00000554139.5:n.398C>G
ENST00000554330.5:n.382C>G
ENST00000554550.5:c.253-159C>G	ENSP00000451435.1:n.253-159C>G
ENST00000554638.5:n.691C>G
ENST00000554897.5:c.253-159C>G	ENSP00000450942.1:n.253-159C>G
ENST00000554944.5:n.415C>G
ENST00000555020.5:n.375C>G
ENST00000555086.5:n.349C>G
ENST00000555214.5:n.262-375C>G
ENST00000556157.1:n.469C>G
ENST00000556244.1:c.332C>G
ENST00000556278.1:c.252+415C>G	ENSP00000451792.1:n.252+415C>G
ENST00000556403.5:n.447C>G
ENST00000556494.5:n.466C>G
ENST00000557541.5:n.489C>G
ENST00000557706.5:n.781C>G
NM_000155.3:c.345C>G	NP_000146.2:p.Pro115=
NM_001258332.1:c.51-159C>G	NP_001245261.1:n.51-159C>G
NM_000155.4:c.345C>G MANE Select	NP_000146.2:p.Pro115=
NM_001258332.2:c.51-159C>G	NP_001245261.1:n.51-159C>G