Canonical Allele Identifier: CA241291

Gene: GALT

Linked Data

• ClinVar Variation Id: 195021
• ClinVar RCV Id: RCV000175532
• dbSNP Id: rs794727235
• gnomAD v4: 9-34647086-C-G
• MyVariant Identifiers: chr9:g.34647083C>G (hg19) ; chr9:g.34647086C>G (hg38)
• PubMed: PMID:23891399

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647086C>G , CM000671.2:g.34647086C>G	GRCh38
NC_000009.11:g.34647083C>G , CM000671.1:g.34647083C>G	GRCh37
NC_000009.10:g.34637083C>G	NCBI36
NG_009029.1:g.5449C>G
NG_009029.2:g.5498C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.83-3C>G	ENSP00000509954.1:n.83-3C>G
ENST00000378842.8:c.83-3C>G MANE Select	ENSP00000368119.4:n.83-3C>G
ENST00000378842.7:c.83-3C>G	ENSP00000368119.3:n.83-3C>G
ENST00000450095.6:c.-120-3C>G	ENSP00000401956.2:n.-120-3C>G
ENST00000465543.6:n.419C>G
ENST00000468099.2:n.155-35C>G
ENST00000472111.5:n.124-3C>G
ENST00000473506.6:c.83-3C>G	ENSP00000432839.2:n.83-3C>G
ENST00000473529.5:n.130-3C>G
ENST00000485531.1:n.76-3C>G
ENST00000487381.5:n.109-3C>G
ENST00000489643.6:n.113-3C>G
ENST00000554085.5:c.83-3C>G	ENSP00000450419.1:n.83-3C>G
ENST00000554139.5:n.136-3C>G
ENST00000554330.5:n.80-3C>G
ENST00000554550.5:c.83-3C>G	ENSP00000451435.1:n.83-3C>G
ENST00000554638.5:n.107-3C>G
ENST00000554897.5:c.83-3C>G	ENSP00000450942.1:n.83-3C>G
ENST00000554944.5:n.113-3C>G
ENST00000555020.5:n.113-3C>G
ENST00000555086.5:n.87-3C>G
ENST00000555214.5:n.92-3C>G
ENST00000556157.1:n.187C>G
ENST00000556278.1:c.83-3C>G	ENSP00000451792.1:n.83-3C>G
ENST00000556403.5:n.96-3C>G
ENST00000556494.5:n.115-3C>G
ENST00000557541.5:n.276-3C>G
ENST00000557706.5:n.194C>G
ENST00000605275.1:n.618C>G
NM_000155.3:c.83-3C>G	NP_000146.2:n.83-3C>G
NM_001258332.1:c.-120-3C>G	NP_001245261.1:n.-120-3C>G
NM_000155.4:c.83-3C>G MANE Select	NP_000146.2:n.83-3C>G
NM_001258332.2:c.-120-3C>G	NP_001245261.1:n.-120-3C>G