Canonical Allele Identifier: CA464403182

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648845T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648848T>G , CM000671.2:g.34648848T>G	GRCh38
NC_000009.11:g.34648845T>G , CM000671.1:g.34648845T>G	GRCh37
NC_000009.10:g.34638845T>G	NCBI36
NG_009029.1:g.7210T>G
NG_028966.1:g.1664T>G
NG_009029.2:g.7260T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*362T>G	ENSP00000509954.1:n.*362T>G
ENST00000378842.8:c.774T>G MANE Select	ENSP00000368119.4:p.Arg258=
ENST00000378842.7:c.774T>G	ENSP00000368119.3:p.Arg258=
ENST00000450095.6:c.447T>G	ENSP00000401956.2:p.Arg149=
ENST00000473506.6:c.*362T>G	ENSP00000432839.2:n.*362T>G
ENST00000489643.6:n.854T>G
ENST00000554085.5:c.*518T>G	ENSP00000450419.1:n.*518T>G
ENST00000554550.5:c.*394T>G	ENSP00000451435.1:n.*394T>G
ENST00000554638.5:n.1246T>G
ENST00000555020.5:n.1235T>G
ENST00000555086.5:n.778T>G
ENST00000555754.1:n.119T>G
ENST00000556244.1:c.761T>G
ENST00000556278.1:c.432+392T>G	ENSP00000451792.1:n.432+392T>G
ENST00000557706.5:n.1336T>G
NM_000155.3:c.774T>G	NP_000146.2:p.Arg258=
NM_001258332.1:c.447T>G	NP_001245261.1:p.Arg149=
NM_000155.4:c.774T>G MANE Select	NP_000146.2:p.Arg258=
NM_001258332.2:c.447T>G	NP_001245261.1:p.Arg149=