Canonical Allele Identifier: CA2689808636

Gene: GALT

Linked Data

• gnomAD v4: 9-34647635-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647635G>A , CM000671.2:g.34647635G>A	GRCh38
NC_000009.11:g.34647632G>A , CM000671.1:g.34647632G>A	GRCh37
NC_000009.10:g.34637632G>A	NCBI36
NG_009029.1:g.5998G>A
NG_028966.1:g.451G>A
NG_009029.2:g.6047G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+68G>A	ENSP00000509954.1:n.328+68G>A
ENST00000378842.8:c.329-22G>A MANE Select	ENSP00000368119.4:n.329-22G>A
ENST00000378842.7:c.329-22G>A	ENSP00000368119.3:n.329-22G>A
ENST00000450095.6:c.51-197G>A	ENSP00000401956.2:n.51-197G>A
ENST00000465543.6:n.668-22G>A
ENST00000472111.5:n.437G>A
ENST00000473506.6:c.280-22G>A	ENSP00000432839.2:n.280-22G>A
ENST00000473529.5:n.443G>A
ENST00000485531.1:n.622G>A
ENST00000487381.5:n.588-22G>A
ENST00000489643.6:n.282+377G>A
ENST00000554085.5:c.*73-22G>A	ENSP00000450419.1:n.*73-22G>A
ENST00000554139.5:n.382-22G>A
ENST00000554330.5:n.344G>A
ENST00000554550.5:c.253-197G>A	ENSP00000451435.1:n.253-197G>A
ENST00000554638.5:n.653G>A
ENST00000554897.5:c.253-197G>A	ENSP00000450942.1:n.253-197G>A
ENST00000554944.5:n.377G>A
ENST00000555020.5:n.359-22G>A
ENST00000555086.5:n.333-22G>A
ENST00000555214.5:n.261+377G>A
ENST00000556157.1:n.453-22G>A
ENST00000556244.1:c.316-22G>A
ENST00000556278.1:c.252+377G>A	ENSP00000451792.1:n.252+377G>A
ENST00000556403.5:n.409G>A
ENST00000556494.5:n.428G>A
ENST00000557541.5:n.473-22G>A
ENST00000557706.5:n.743G>A
NM_000155.3:c.329-22G>A	NP_000146.2:n.329-22G>A
NM_001258332.1:c.51-197G>A	NP_001245261.1:n.51-197G>A
NM_000155.4:c.329-22G>A MANE Select	NP_000146.2:n.329-22G>A
NM_001258332.2:c.51-197G>A	NP_001245261.1:n.51-197G>A