Canonical Allele Identifier: CA464402098

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648369T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648372T>G , CM000671.2:g.34648372T>G	GRCh38
NC_000009.11:g.34648369T>G , CM000671.1:g.34648369T>G	GRCh37
NC_000009.10:g.34638369T>G	NCBI36
NG_009029.1:g.6735T>G
NG_028966.1:g.1188T>G
NG_009029.2:g.6784T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*191T>G	ENSP00000509954.1:n.*191T>G
ENST00000378842.8:c.603T>G MANE Select	ENSP00000368119.4:p.Arg201=
ENST00000378842.7:c.603T>G	ENSP00000368119.3:p.Arg201=
ENST00000450095.6:c.276T>G	ENSP00000401956.2:p.Arg92=
ENST00000472111.5:n.859T>G
ENST00000473506.6:c.*191T>G	ENSP00000432839.2:n.*191T>G
ENST00000473529.5:n.762T>G
ENST00000485531.1:n.1197T>G
ENST00000487381.5:n.988T>G
ENST00000489643.6:n.378T>G
ENST00000554085.5:c.*347T>G	ENSP00000450419.1:n.*347T>G
ENST00000554139.5:n.849T>G
ENST00000554550.5:c.*223T>G	ENSP00000451435.1:n.*223T>G
ENST00000554638.5:n.1075T>G
ENST00000554897.5:c.*290T>G	ENSP00000450942.1:n.*290T>G
ENST00000554944.5:n.952T>G
ENST00000555020.5:n.759T>G
ENST00000555086.5:n.607T>G
ENST00000555214.5:n.424T>G
ENST00000556244.1:c.590T>G
ENST00000556278.1:c.348T>G	ENSP00000451792.1:p.Arg116=
ENST00000556494.5:n.724T>G
ENST00000557706.5:n.1165T>G
NM_000155.3:c.603T>G	NP_000146.2:p.Arg201=
NM_001258332.1:c.276T>G	NP_001245261.1:p.Arg92=
NM_000155.4:c.603T>G MANE Select	NP_000146.2:p.Arg201=
NM_001258332.2:c.276T>G	NP_001245261.1:p.Arg92=