Canonical Allele Identifier: CA464403048

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648812A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648815A>G , CM000671.2:g.34648815A>G	GRCh38
NC_000009.11:g.34648812A>G , CM000671.1:g.34648812A>G	GRCh37
NC_000009.10:g.34638812A>G	NCBI36
NG_009029.1:g.7178A>G
NG_028966.1:g.1631A>G
NG_009029.2:g.7227A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*329A>G	ENSP00000509954.1:n.*329A>G
ENST00000378842.8:c.741A>G MANE Select	ENSP00000368119.4:p.Ala247=
ENST00000378842.7:c.741A>G	ENSP00000368119.3:p.Ala247=
ENST00000450095.6:c.414A>G	ENSP00000401956.2:p.Ala138=
ENST00000473506.6:c.*329A>G	ENSP00000432839.2:n.*329A>G
ENST00000473529.5:n.900A>G
ENST00000487381.5:n.1431A>G
ENST00000489643.6:n.821A>G
ENST00000554085.5:c.*485A>G	ENSP00000450419.1:n.*485A>G
ENST00000554550.5:c.*361A>G	ENSP00000451435.1:n.*361A>G
ENST00000554638.5:n.1213A>G
ENST00000555020.5:n.1202A>G
ENST00000555086.5:n.745A>G
ENST00000555754.1:n.86A>G
ENST00000556244.1:c.728A>G
ENST00000556278.1:c.432+359A>G	ENSP00000451792.1:n.432+359A>G
ENST00000557706.5:n.1303A>G
NM_000155.3:c.741A>G	NP_000146.2:p.Ala247=
NM_001258332.1:c.414A>G	NP_001245261.1:p.Ala138=
NM_000155.4:c.741A>G MANE Select	NP_000146.2:p.Ala247=
NM_001258332.2:c.414A>G	NP_001245261.1:p.Ala138=