Canonical Allele Identifier: CA464403185

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648846C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648849C>A , CM000671.2:g.34648849C>A	GRCh38
NC_000009.11:g.34648846C>A , CM000671.1:g.34648846C>A	GRCh37
NC_000009.10:g.34638846C>A	NCBI36
NG_009029.1:g.7211C>A
NG_028966.1:g.1665C>A
NG_009029.2:g.7261C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*363C>A	ENSP00000509954.1:n.*363C>A
ENST00000378842.8:c.775C>A MANE Select	ENSP00000368119.4:p.Arg259=
ENST00000378842.7:c.775C>A	ENSP00000368119.3:p.Arg259=
ENST00000450095.6:c.448C>A	ENSP00000401956.2:p.Arg150=
ENST00000473506.6:c.*363C>A	ENSP00000432839.2:n.*363C>A
ENST00000489643.6:n.855C>A
ENST00000554085.5:c.*519C>A	ENSP00000450419.1:n.*519C>A
ENST00000554550.5:c.*395C>A	ENSP00000451435.1:n.*395C>A
ENST00000554638.5:n.1247C>A
ENST00000555020.5:n.1236C>A
ENST00000555086.5:n.779C>A
ENST00000555754.1:n.120C>A
ENST00000556244.1:c.762C>A
ENST00000556278.1:c.432+393C>A	ENSP00000451792.1:n.432+393C>A
ENST00000557706.5:n.1337C>A
NM_000155.3:c.775C>A	NP_000146.2:p.Arg259=
NM_001258332.1:c.448C>A	NP_001245261.1:p.Arg150=
NM_000155.4:c.775C>A MANE Select	NP_000146.2:p.Arg259=
NM_001258332.2:c.448C>A	NP_001245261.1:p.Arg150=