Canonical Allele Identifier: CA464404387

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649501G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649504G>A , CM000671.2:g.34649504G>A	GRCh38
NC_000009.11:g.34649501G>A , CM000671.1:g.34649501G>A	GRCh37
NC_000009.10:g.34639501G>A	NCBI36
NG_009029.1:g.7867G>A
NG_028966.1:g.2320G>A
NG_009029.2:g.7916G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*587G>A	ENSP00000509954.1:n.*587G>A
ENST00000378842.8:c.999G>A MANE Select	ENSP00000368119.4:p.Arg333=
ENST00000378842.7:c.999G>A	ENSP00000368119.3:p.Arg333=
ENST00000450095.6:c.672G>A	ENSP00000401956.2:p.Arg224=
ENST00000488412.2:n.583G>A
ENST00000489643.6:n.1407G>A
ENST00000554550.5:c.*619G>A	ENSP00000451435.1:n.*619G>A
ENST00000554638.5:n.1471G>A
ENST00000555020.5:n.1788G>A
ENST00000555754.1:n.447G>A
ENST00000556278.1:c.432+1048G>A	ENSP00000451792.1:n.432+1048G>A
ENST00000557706.5:n.1574G>A
NM_000155.3:c.999G>A	NP_000146.2:p.Arg333=
NM_001258332.1:c.672G>A	NP_001245261.1:p.Arg224=
NM_000155.4:c.999G>A MANE Select	NP_000146.2:p.Arg333=
NM_001258332.2:c.672G>A	NP_001245261.1:p.Arg224=