Canonical Allele Identifier: CA373285237

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649538C>A (hg19) ; chr9:g.34649541C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649541C>A , CM000671.2:g.34649541C>A	GRCh38
NC_000009.11:g.34649538C>A , CM000671.1:g.34649538C>A	GRCh37
NC_000009.10:g.34639538C>A	NCBI36
NG_009029.1:g.7904C>A
NG_028966.1:g.2357C>A
NG_009029.2:g.7953C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*624C>A	ENSP00000509954.1:n.*624C>A
ENST00000378842.8:c.1036C>A MANE Select	ENSP00000368119.4:p.Gln346Lys
ENST00000378842.7:c.1036C>A	ENSP00000368119.3:p.Gln346Lys
ENST00000450095.6:c.709C>A	ENSP00000401956.2:p.Gln237Lys
ENST00000488412.2:n.620C>A
ENST00000489643.6:n.1444C>A
ENST00000554550.5:c.*656C>A	ENSP00000451435.1:n.*656C>A
ENST00000554638.5:n.1508C>A
ENST00000555020.5:n.1825C>A
ENST00000555754.1:n.484C>A
ENST00000556278.1:c.432+1085C>A	ENSP00000451792.1:n.432+1085C>A
ENST00000557706.5:n.1611C>A
NM_000155.3:c.1036C>A	NP_000146.2:p.Gln346Lys
NM_001258332.1:c.709C>A	NP_001245261.1:p.Gln237Lys
NM_000155.4:c.1036C>A MANE Select	NP_000146.2:p.Gln346Lys
NM_001258332.2:c.709C>A	NP_001245261.1:p.Gln237Lys