Canonical Allele Identifier: CA2689809173
Gene: GALT HGNC NCBI

Linked Data

gnomAD v4: 9-34648560-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648560A>T , CM000671.2:g.34648560A>T GRCh38
NC_000009.11:g.34648557A>T , CM000671.1:g.34648557A>T GRCh37
NC_000009.10:g.34638557A>T NCBI36
NG_009029.1:g.6923A>T
NG_028966.1:g.1376A>T
NG_009029.2:g.6972A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.*275+104A>T ENSP00000509954.1:n.*275+104A>T
ENST00000378842.8:c.687+104A>T MANE Select ENSP00000368119.4:n.687+104A>T
ENST00000378842.7:c.687+104A>T ENSP00000368119.3:n.687+104A>T
ENST00000450095.6:c.360+104A>T ENSP00000401956.2:n.360+104A>T
ENST00000473506.6:c.*275+104A>T ENSP00000432839.2:n.*275+104A>T
ENST00000473529.5:n.846+104A>T
ENST00000487381.5:n.1176A>T
ENST00000489643.6:n.566A>T
ENST00000554085.5:c.*431+104A>T ENSP00000450419.1:n.*431+104A>T
ENST00000554550.5:c.*307+104A>T ENSP00000451435.1:n.*307+104A>T
ENST00000554638.5:n.1159+104A>T
ENST00000555020.5:n.947A>T
ENST00000555086.5:n.691+104A>T
ENST00000555214.5:n.612A>T
ENST00000555754.1:n.32+104A>T
ENST00000556244.1:c.674+104A>T
ENST00000556278.1:c.432+104A>T ENSP00000451792.1:n.432+104A>T
ENST00000557706.5:n.1249+104A>T
NM_000155.3:c.687+104A>T NP_000146.2:n.687+104A>T
NM_001258332.1:c.360+104A>T NP_001245261.1:n.360+104A>T
NM_000155.4:c.687+104A>T MANE Select NP_000146.2:n.687+104A>T
NM_001258332.2:c.360+104A>T NP_001245261.1:n.360+104A>T