Canonical Allele Identifier: CA373281895

Gene: GALT

Linked Data

• gnomAD v4: 9-34648350-T-G
• MyVariant Identifiers: chr9:g.34648347T>G (hg19) ; chr9:g.34648350T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648350T>G , CM000671.2:g.34648350T>G	GRCh38
NC_000009.11:g.34648347T>G , CM000671.1:g.34648347T>G	GRCh37
NC_000009.10:g.34638347T>G	NCBI36
NG_009029.1:g.6713T>G
NG_028966.1:g.1166T>G
NG_009029.2:g.6762T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*169T>G	ENSP00000509954.1:n.*169T>G
ENST00000378842.8:c.581T>G MANE Select	ENSP00000368119.4:p.Phe194Cys
ENST00000378842.7:c.581T>G	ENSP00000368119.3:p.Phe194Cys
ENST00000450095.6:c.254T>G	ENSP00000401956.2:p.Phe85Cys
ENST00000472111.5:n.837T>G
ENST00000473506.6:c.*169T>G	ENSP00000432839.2:n.*169T>G
ENST00000473529.5:n.740T>G
ENST00000485531.1:n.1175T>G
ENST00000487381.5:n.966T>G
ENST00000489643.6:n.356T>G
ENST00000554085.5:c.*325T>G	ENSP00000450419.1:n.*325T>G
ENST00000554139.5:n.827T>G
ENST00000554550.5:c.*201T>G	ENSP00000451435.1:n.*201T>G
ENST00000554638.5:n.1053T>G
ENST00000554897.5:c.*268T>G	ENSP00000450942.1:n.*268T>G
ENST00000554944.5:n.930T>G
ENST00000555020.5:n.737T>G
ENST00000555086.5:n.585T>G
ENST00000555214.5:n.402T>G
ENST00000556244.1:c.568T>G
ENST00000556278.1:c.326T>G	ENSP00000451792.1:p.Phe109Cys
ENST00000556494.5:n.702T>G
ENST00000557706.5:n.1143T>G
NM_000155.3:c.581T>G	NP_000146.2:p.Phe194Cys
NM_001258332.1:c.254T>G	NP_001245261.1:p.Phe85Cys
NM_000155.4:c.581T>G MANE Select	NP_000146.2:p.Phe194Cys
NM_001258332.2:c.254T>G	NP_001245261.1:p.Phe85Cys