Canonical Allele Identifier: CA1845639332

Gene: GALT

Linked Data

• dbSNP Id: rs1587239592

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648643T>G , CM000671.2:g.34648643T>G	GRCh38
NC_000009.11:g.34648640T>G , CM000671.1:g.34648640T>G	GRCh37
NC_000009.10:g.34638640T>G	NCBI36
NG_009029.1:g.7006T>G
NG_028966.1:g.1459T>G
NG_009029.2:g.7055T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*276-119T>G	ENSP00000509954.1:n.*276-119T>G
ENST00000378842.8:c.688-119T>G MANE Select	ENSP00000368119.4:n.688-119T>G
ENST00000378842.7:c.688-119T>G	ENSP00000368119.3:n.688-119T>G
ENST00000450095.6:c.361-119T>G	ENSP00000401956.2:n.361-119T>G
ENST00000473506.6:c.*276-119T>G	ENSP00000432839.2:n.*276-119T>G
ENST00000473529.5:n.847-119T>G
ENST00000487381.5:n.1259T>G
ENST00000489643.6:n.649T>G
ENST00000554085.5:c.*432-119T>G	ENSP00000450419.1:n.*432-119T>G
ENST00000554550.5:c.*308-119T>G	ENSP00000451435.1:n.*308-119T>G
ENST00000554638.5:n.1160-119T>G
ENST00000555020.5:n.1030T>G
ENST00000555086.5:n.692-119T>G
ENST00000555754.1:n.33-119T>G
ENST00000556244.1:c.675-119T>G
ENST00000556278.1:c.432+187T>G	ENSP00000451792.1:n.432+187T>G
ENST00000557706.5:n.1250-119T>G
NM_000155.3:c.688-119T>G	NP_000146.2:n.688-119T>G
NM_001258332.1:c.361-119T>G	NP_001245261.1:n.361-119T>G
NM_000155.4:c.688-119T>G MANE Select	NP_000146.2:n.688-119T>G
NM_001258332.2:c.361-119T>G	NP_001245261.1:n.361-119T>G