Canonical Allele Identifier: CA2689808572
Gene: GALT HGNC NCBI

Linked Data

gnomAD v4: 9-34647322-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647322T>C , CM000671.2:g.34647322T>C GRCh38
NC_000009.11:g.34647319T>C , CM000671.1:g.34647319T>C GRCh37
NC_000009.10:g.34637319T>C NCBI36
NG_009029.1:g.5685T>C
NG_028966.1:g.138T>C
NG_009029.2:g.5734T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.252+64T>C ENSP00000509954.1:n.252+64T>C
ENST00000378842.8:c.252+64T>C MANE Select ENSP00000368119.4:n.252+64T>C
ENST00000378842.7:c.252+64T>C ENSP00000368119.3:n.252+64T>C
ENST00000450095.6:c.50+64T>C ENSP00000401956.2:n.50+64T>C
ENST00000465543.6:n.591+64T>C
ENST00000468099.2:n.356T>C
ENST00000472111.5:n.293+64T>C
ENST00000473506.6:c.252+64T>C ENSP00000432839.2:n.252+64T>C
ENST00000473529.5:n.299+64T>C
ENST00000485531.1:n.309T>C
ENST00000487381.5:n.342T>C
ENST00000489643.6:n.282+64T>C
ENST00000554085.5:c.252+64T>C ENSP00000450419.1:n.252+64T>C
ENST00000554139.5:n.305+64T>C
ENST00000554330.5:n.249+64T>C
ENST00000554550.5:c.252+64T>C ENSP00000451435.1:n.252+64T>C
ENST00000554638.5:n.340T>C
ENST00000554897.5:c.252+64T>C ENSP00000450942.1:n.252+64T>C
ENST00000554944.5:n.282+64T>C
ENST00000555020.5:n.282+64T>C
ENST00000555086.5:n.256+64T>C
ENST00000555214.5:n.261+64T>C
ENST00000556157.1:n.359+64T>C
ENST00000556244.1:c.136+64T>C
ENST00000556278.1:c.252+64T>C ENSP00000451792.1:n.252+64T>C
ENST00000556403.5:n.265+64T>C
ENST00000556494.5:n.284+64T>C
ENST00000557541.5:n.445+64T>C
ENST00000557706.5:n.430T>C
NM_000155.3:c.252+64T>C NP_000146.2:n.252+64T>C
NM_001258332.1:c.50+64T>C NP_001245261.1:n.50+64T>C
NM_000155.4:c.252+64T>C MANE Select NP_000146.2:n.252+64T>C
NM_001258332.2:c.50+64T>C NP_001245261.1:n.50+64T>C