Canonical Allele Identifier: CA1845635857
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1564100792
gnomAD v4: 9-34647285-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647285A>T , CM000671.2:g.34647285A>T GRCh38
NC_000009.11:g.34647282A>T , CM000671.1:g.34647282A>T GRCh37
NC_000009.10:g.34637282A>T NCBI36
NG_009029.1:g.5648A>T
NG_028966.1:g.101A>T
NG_009029.2:g.5697A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.252+27A>T ENSP00000509954.1:n.252+27A>T
ENST00000378842.8:c.252+27A>T MANE Select ENSP00000368119.4:n.252+27A>T
ENST00000378842.7:c.252+27A>T ENSP00000368119.3:n.252+27A>T
ENST00000450095.6:c.50+27A>T ENSP00000401956.2:n.50+27A>T
ENST00000465543.6:n.591+27A>T
ENST00000468099.2:n.319A>T
ENST00000472111.5:n.293+27A>T
ENST00000473506.6:c.252+27A>T ENSP00000432839.2:n.252+27A>T
ENST00000473529.5:n.299+27A>T
ENST00000485531.1:n.272A>T
ENST00000487381.5:n.305A>T
ENST00000489643.6:n.282+27A>T
ENST00000554085.5:c.252+27A>T ENSP00000450419.1:n.252+27A>T
ENST00000554139.5:n.305+27A>T
ENST00000554330.5:n.249+27A>T
ENST00000554550.5:c.252+27A>T ENSP00000451435.1:n.252+27A>T
ENST00000554638.5:n.303A>T
ENST00000554897.5:c.252+27A>T ENSP00000450942.1:n.252+27A>T
ENST00000554944.5:n.282+27A>T
ENST00000555020.5:n.282+27A>T
ENST00000555086.5:n.256+27A>T
ENST00000555214.5:n.261+27A>T
ENST00000556157.1:n.359+27A>T
ENST00000556244.1:c.136+27A>T
ENST00000556278.1:c.252+27A>T ENSP00000451792.1:n.252+27A>T
ENST00000556403.5:n.265+27A>T
ENST00000556494.5:n.284+27A>T
ENST00000557541.5:n.445+27A>T
ENST00000557706.5:n.393A>T
NM_000155.3:c.252+27A>T NP_000146.2:n.252+27A>T
NM_001258332.1:c.50+27A>T NP_001245261.1:n.50+27A>T
NM_000155.4:c.252+27A>T MANE Select NP_000146.2:n.252+27A>T
NM_001258332.2:c.50+27A>T NP_001245261.1:n.50+27A>T