Canonical Allele Identifier: CA1845639201
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1821169157
gnomAD v4: 9-34648510-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648510A>G , CM000671.2:g.34648510A>G GRCh38
NC_000009.11:g.34648507A>G , CM000671.1:g.34648507A>G GRCh37
NC_000009.10:g.34638507A>G NCBI36
NG_009029.1:g.6873A>G
NG_028966.1:g.1326A>G
NG_009029.2:g.6922A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.*275+54A>G ENSP00000509954.1:n.*275+54A>G
ENST00000378842.8:c.687+54A>G MANE Select ENSP00000368119.4:n.687+54A>G
ENST00000378842.7:c.687+54A>G ENSP00000368119.3:n.687+54A>G
ENST00000450095.6:c.360+54A>G ENSP00000401956.2:n.360+54A>G
ENST00000473506.6:c.*275+54A>G ENSP00000432839.2:n.*275+54A>G
ENST00000473529.5:n.846+54A>G
ENST00000487381.5:n.1126A>G
ENST00000489643.6:n.516A>G
ENST00000554085.5:c.*431+54A>G ENSP00000450419.1:n.*431+54A>G
ENST00000554550.5:c.*307+54A>G ENSP00000451435.1:n.*307+54A>G
ENST00000554638.5:n.1159+54A>G
ENST00000555020.5:n.897A>G
ENST00000555086.5:n.691+54A>G
ENST00000555214.5:n.562A>G
ENST00000555754.1:n.32+54A>G
ENST00000556244.1:c.674+54A>G
ENST00000556278.1:c.432+54A>G ENSP00000451792.1:n.432+54A>G
ENST00000556494.5:n.862A>G
ENST00000557706.5:n.1249+54A>G
NM_000155.3:c.687+54A>G NP_000146.2:n.687+54A>G
NM_001258332.1:c.360+54A>G NP_001245261.1:n.360+54A>G
NM_000155.4:c.687+54A>G MANE Select NP_000146.2:n.687+54A>G
NM_001258332.2:c.360+54A>G NP_001245261.1:n.360+54A>G