Canonical Allele Identifier: CA5036083

Gene: GALT

Linked Data

• dbSNP Id: rs768894080
• ExAC: 9:34647570 C / G
• gnomAD v2: 9-34647570-C-G
• MyVariant Identifiers: chr9:g.34647570C>G (hg19) ; chr9:g.34647573C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647573C>G , CM000671.2:g.34647573C>G	GRCh38
NC_000009.11:g.34647570C>G , CM000671.1:g.34647570C>G	GRCh37
NC_000009.10:g.34637570C>G	NCBI36
NG_009029.1:g.5936C>G
NG_028966.1:g.389C>G
NG_009029.2:g.5985C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.328+6C>G	ENSP00000509954.1:n.328+6C>G
ENST00000378842.8:c.328+6C>G MANE Select	ENSP00000368119.4:n.328+6C>G
ENST00000378842.7:c.328+6C>G	ENSP00000368119.3:n.328+6C>G
ENST00000450095.6:c.51-259C>G	ENSP00000401956.2:n.51-259C>G
ENST00000465543.6:n.667+6C>G
ENST00000472111.5:n.375C>G
ENST00000473506.6:c.279+6C>G	ENSP00000432839.2:n.279+6C>G
ENST00000473529.5:n.381C>G
ENST00000485531.1:n.560C>G
ENST00000487381.5:n.587+6C>G
ENST00000489643.6:n.282+315C>G
ENST00000554085.5:c.*72+6C>G	ENSP00000450419.1:n.*72+6C>G
ENST00000554139.5:n.381+6C>G
ENST00000554330.5:n.282C>G
ENST00000554550.5:c.253-259C>G	ENSP00000451435.1:n.253-259C>G
ENST00000554638.5:n.591C>G
ENST00000554897.5:c.253-259C>G	ENSP00000450942.1:n.253-259C>G
ENST00000554944.5:n.315C>G
ENST00000555020.5:n.358+6C>G
ENST00000555086.5:n.332+6C>G
ENST00000555214.5:n.261+315C>G
ENST00000556157.1:n.452+6C>G
ENST00000556244.1:c.315+6C>G
ENST00000556278.1:c.252+315C>G	ENSP00000451792.1:n.252+315C>G
ENST00000556403.5:n.347C>G
ENST00000556494.5:n.366C>G
ENST00000557541.5:n.472+6C>G
ENST00000557706.5:n.681C>G
NM_000155.3:c.328+6C>G	NP_000146.2:n.328+6C>G
NM_001258332.1:c.51-259C>G	NP_001245261.1:n.51-259C>G
NM_000155.4:c.328+6C>G MANE Select	NP_000146.2:n.328+6C>G
NM_001258332.2:c.51-259C>G	NP_001245261.1:n.51-259C>G