Canonical Allele Identifier: CA2783504154
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646841C>T , CM000671.2:g.34646841C>T GRCh38
NC_000009.11:g.34646838C>T , CM000671.1:g.34646838C>T GRCh37
NC_000009.10:g.34636838C>T NCBI36
NG_009029.1:g.5204C>T
NG_009029.2:g.5253C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.82+55C>T ENSP00000509954.1:n.82+55C>T
ENST00000378842.8:c.82+55C>T MANE Select ENSP00000368119.4:n.82+55C>T
ENST00000378842.7:c.82+55C>T ENSP00000368119.3:n.82+55C>T
ENST00000450095.6:c.-121+55C>T ENSP00000401956.2:n.-121+55C>T
ENST00000465543.6:n.174C>T
ENST00000468099.2:n.154+55C>T
ENST00000472111.5:n.123+55C>T
ENST00000473506.6:c.82+55C>T ENSP00000432839.2:n.82+55C>T
ENST00000473529.5:n.129+55C>T
ENST00000487381.5:n.108+55C>T
ENST00000489643.6:n.112+55C>T
ENST00000554085.5:c.82+55C>T ENSP00000450419.1:n.82+55C>T
ENST00000554139.5:n.135+55C>T
ENST00000554330.5:n.53C>T
ENST00000554550.5:c.82+55C>T ENSP00000451435.1:n.82+55C>T
ENST00000554638.5:n.106+55C>T
ENST00000554897.5:c.82+55C>T ENSP00000450942.1:n.82+55C>T
ENST00000554944.5:n.112+55C>T
ENST00000555020.5:n.112+55C>T
ENST00000555086.5:n.60C>T
ENST00000555214.5:n.91+55C>T
ENST00000556278.1:c.82+55C>T ENSP00000451792.1:n.82+55C>T
ENST00000556403.5:n.69C>T
ENST00000556494.5:n.36C>T
ENST00000557541.5:n.197C>T
ENST00000605275.1:n.373C>T
NM_000155.3:c.82+55C>T NP_000146.2:n.82+55C>T
NM_001258332.1:c.-121+55C>T NP_001245261.1:n.-121+55C>T
NM_000155.4:c.82+55C>T MANE Select NP_000146.2:n.82+55C>T
NM_001258332.2:c.-121+55C>T NP_001245261.1:n.-121+55C>T