Canonical Allele Identifier: CA373278457

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647087C>G (hg19) ; chr9:g.34647090C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647090C>G , CM000671.2:g.34647090C>G	GRCh38
NC_000009.11:g.34647087C>G , CM000671.1:g.34647087C>G	GRCh37
NC_000009.10:g.34637087C>G	NCBI36
NG_009029.1:g.5453C>G
NG_009029.2:g.5502C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.84C>G	ENSP00000509954.1:p.Asp28Glu
ENST00000378842.8:c.84C>G MANE Select	ENSP00000368119.4:p.Asp28Glu
ENST00000378842.7:c.84C>G	ENSP00000368119.3:p.Asp28Glu
ENST00000450095.6:c.-119C>G	ENSP00000401956.2:n.-119C>G
ENST00000465543.6:n.423C>G
ENST00000468099.2:n.155-31C>G
ENST00000472111.5:n.125C>G
ENST00000473506.6:c.84C>G	ENSP00000432839.2:p.Asp28Glu
ENST00000473529.5:n.131C>G
ENST00000485531.1:n.77C>G
ENST00000487381.5:n.110C>G
ENST00000489643.6:n.114C>G
ENST00000554085.5:c.84C>G	ENSP00000450419.1:p.Asp28Glu
ENST00000554139.5:n.137C>G
ENST00000554330.5:n.81C>G
ENST00000554550.5:c.84C>G	ENSP00000451435.1:p.Asp28Glu
ENST00000554638.5:n.108C>G
ENST00000554897.5:c.84C>G	ENSP00000450942.1:p.Asp28Glu
ENST00000554944.5:n.114C>G
ENST00000555020.5:n.114C>G
ENST00000555086.5:n.88C>G
ENST00000555214.5:n.93C>G
ENST00000556157.1:n.191C>G
ENST00000556278.1:c.84C>G	ENSP00000451792.1:p.Asp28Glu
ENST00000556403.5:n.97C>G
ENST00000556494.5:n.116C>G
ENST00000557541.5:n.277C>G
ENST00000557706.5:n.198C>G
ENST00000605275.1:n.622C>G
NM_000155.3:c.84C>G	NP_000146.2:p.Asp28Glu
NM_001258332.1:c.-119C>G	NP_001245261.1:n.-119C>G
NM_000155.4:c.84C>G MANE Select	NP_000146.2:p.Asp28Glu
NM_001258332.2:c.-119C>G	NP_001245261.1:n.-119C>G