Canonical Allele Identifier: CA373284490

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649064C>G (hg19) ; chr9:g.34649067C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649067C>G , CM000671.2:g.34649067C>G	GRCh38
NC_000009.11:g.34649064C>G , CM000671.1:g.34649064C>G	GRCh37
NC_000009.10:g.34639064C>G	NCBI36
NG_009029.1:g.7430C>G
NG_028966.1:g.1883C>G
NG_009029.2:g.7479C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*478C>G	ENSP00000509954.1:n.*478C>G
ENST00000378842.8:c.890C>G MANE Select	ENSP00000368119.4:p.Ser297Cys
ENST00000378842.7:c.890C>G	ENSP00000368119.3:p.Ser297Cys
ENST00000450095.6:c.563C>G	ENSP00000401956.2:p.Ser188Cys
ENST00000488412.2:n.146C>G
ENST00000489643.6:n.970C>G
ENST00000554550.5:c.*510C>G	ENSP00000451435.1:n.*510C>G
ENST00000554638.5:n.1362C>G
ENST00000555020.5:n.1351C>G
ENST00000555086.5:n.997C>G
ENST00000555754.1:n.338C>G
ENST00000556278.1:c.432+611C>G	ENSP00000451792.1:n.432+611C>G
ENST00000557706.5:n.1465C>G
NM_000155.3:c.890C>G	NP_000146.2:p.Ser297Cys
NM_001258332.1:c.563C>G	NP_001245261.1:p.Ser188Cys
NM_000155.4:c.890C>G MANE Select	NP_000146.2:p.Ser297Cys
NM_001258332.2:c.563C>G	NP_001245261.1:p.Ser188Cys