Canonical Allele Identifier: CA2689809076

Gene: GALT

Linked Data

• gnomAD v4: 9-34648486-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648486A>G , CM000671.2:g.34648486A>G	GRCh38
NC_000009.11:g.34648483A>G , CM000671.1:g.34648483A>G	GRCh37
NC_000009.10:g.34638483A>G	NCBI36
NG_009029.1:g.6849A>G
NG_028966.1:g.1302A>G
NG_009029.2:g.6898A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*275+30A>G	ENSP00000509954.1:n.*275+30A>G
ENST00000378842.8:c.687+30A>G MANE Select	ENSP00000368119.4:n.687+30A>G
ENST00000378842.7:c.687+30A>G	ENSP00000368119.3:n.687+30A>G
ENST00000450095.6:c.360+30A>G	ENSP00000401956.2:n.360+30A>G
ENST00000472111.5:n.973A>G
ENST00000473506.6:c.*275+30A>G	ENSP00000432839.2:n.*275+30A>G
ENST00000473529.5:n.846+30A>G
ENST00000487381.5:n.1102A>G
ENST00000489643.6:n.492A>G
ENST00000554085.5:c.*431+30A>G	ENSP00000450419.1:n.*431+30A>G
ENST00000554550.5:c.*307+30A>G	ENSP00000451435.1:n.*307+30A>G
ENST00000554638.5:n.1159+30A>G
ENST00000555020.5:n.873A>G
ENST00000555086.5:n.691+30A>G
ENST00000555214.5:n.538A>G
ENST00000555754.1:n.32+30A>G
ENST00000556244.1:c.674+30A>G
ENST00000556278.1:c.432+30A>G	ENSP00000451792.1:n.432+30A>G
ENST00000556494.5:n.838A>G
ENST00000557706.5:n.1249+30A>G
NM_000155.3:c.687+30A>G	NP_000146.2:n.687+30A>G
NM_001258332.1:c.360+30A>G	NP_001245261.1:n.360+30A>G
NM_000155.4:c.687+30A>G MANE Select	NP_000146.2:n.687+30A>G
NM_001258332.2:c.360+30A>G	NP_001245261.1:n.360+30A>G