Canonical Allele Identifier: CA2689808582

Gene: GALT

Linked Data

• gnomAD v4: 9-34647344-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647344A>G , CM000671.2:g.34647344A>G	GRCh38
NC_000009.11:g.34647341A>G , CM000671.1:g.34647341A>G	GRCh37
NC_000009.10:g.34637341A>G	NCBI36
NG_009029.1:g.5707A>G
NG_028966.1:g.160A>G
NG_009029.2:g.5756A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.252+86A>G	ENSP00000509954.1:n.252+86A>G
ENST00000378842.8:c.252+86A>G MANE Select	ENSP00000368119.4:n.252+86A>G
ENST00000378842.7:c.252+86A>G	ENSP00000368119.3:n.252+86A>G
ENST00000450095.6:c.50+86A>G	ENSP00000401956.2:n.50+86A>G
ENST00000465543.6:n.591+86A>G
ENST00000468099.2:n.378A>G
ENST00000472111.5:n.293+86A>G
ENST00000473506.6:c.252+86A>G	ENSP00000432839.2:n.252+86A>G
ENST00000473529.5:n.299+86A>G
ENST00000485531.1:n.331A>G
ENST00000487381.5:n.364A>G
ENST00000489643.6:n.282+86A>G
ENST00000554085.5:c.252+86A>G	ENSP00000450419.1:n.252+86A>G
ENST00000554139.5:n.305+86A>G
ENST00000554330.5:n.249+86A>G
ENST00000554550.5:c.252+86A>G	ENSP00000451435.1:n.252+86A>G
ENST00000554638.5:n.362A>G
ENST00000554897.5:c.252+86A>G	ENSP00000450942.1:n.252+86A>G
ENST00000554944.5:n.282+86A>G
ENST00000555020.5:n.282+86A>G
ENST00000555086.5:n.256+86A>G
ENST00000555214.5:n.261+86A>G
ENST00000556157.1:n.359+86A>G
ENST00000556244.1:c.137-45A>G
ENST00000556278.1:c.252+86A>G	ENSP00000451792.1:n.252+86A>G
ENST00000556403.5:n.265+86A>G
ENST00000556494.5:n.284+86A>G
ENST00000557541.5:n.445+86A>G
ENST00000557706.5:n.452A>G
NM_000155.3:c.252+86A>G	NP_000146.2:n.252+86A>G
NM_001258332.1:c.50+86A>G	NP_001245261.1:n.50+86A>G
NM_000155.4:c.252+86A>G MANE Select	NP_000146.2:n.252+86A>G
NM_001258332.2:c.50+86A>G	NP_001245261.1:n.50+86A>G