Canonical Allele Identifier: CA373278841

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647237C>G (hg19) ; chr9:g.34647240C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647240C>G , CM000671.2:g.34647240C>G	GRCh38
NC_000009.11:g.34647237C>G , CM000671.1:g.34647237C>G	GRCh37
NC_000009.10:g.34637237C>G	NCBI36
NG_009029.1:g.5603C>G
NG_028966.1:g.56C>G
NG_009029.2:g.5652C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.234C>G	ENSP00000509954.1:p.Ala78=
ENST00000378842.8:c.234C>G MANE Select	ENSP00000368119.4:p.Ala78=
ENST00000378842.7:c.234C>G	ENSP00000368119.3:p.Ala78=
ENST00000450095.6:c.32C>G	ENSP00000401956.2:p.Pro11Arg
ENST00000465543.6:n.573C>G
ENST00000468099.2:n.274C>G
ENST00000472111.5:n.275C>G
ENST00000473506.6:c.234C>G	ENSP00000432839.2:p.Ala78=
ENST00000473529.5:n.281C>G
ENST00000485531.1:n.227C>G
ENST00000487381.5:n.260C>G
ENST00000489643.6:n.264C>G
ENST00000554085.5:c.234C>G	ENSP00000450419.1:p.Ala78=
ENST00000554139.5:n.287C>G
ENST00000554330.5:n.231C>G
ENST00000554550.5:c.234C>G	ENSP00000451435.1:p.Ala78=
ENST00000554638.5:n.258C>G
ENST00000554897.5:c.234C>G	ENSP00000450942.1:p.Ala78=
ENST00000554944.5:n.264C>G
ENST00000555020.5:n.264C>G
ENST00000555086.5:n.238C>G
ENST00000555214.5:n.243C>G
ENST00000556157.1:n.341C>G
ENST00000556244.1:c.118C>G
ENST00000556278.1:c.234C>G	ENSP00000451792.1:p.Ala78=
ENST00000556403.5:n.247C>G
ENST00000556494.5:n.266C>G
ENST00000557541.5:n.427C>G
ENST00000557706.5:n.348C>G
NM_000155.3:c.234C>G	NP_000146.2:p.Ala78=
NM_001258332.1:c.32C>G	NP_001245261.1:p.Pro11Arg
NM_000155.4:c.234C>G MANE Select	NP_000146.2:p.Ala78=
NM_001258332.2:c.32C>G	NP_001245261.1:p.Pro11Arg