Canonical Allele Identifier: CA2524601868

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648966A>G , CM000671.2:g.34648966A>G	GRCh38
NC_000009.11:g.34648963A>G , CM000671.1:g.34648963A>G	GRCh37
NC_000009.10:g.34638963A>G	NCBI36
NG_009029.1:g.7329A>G
NG_028966.1:g.1782A>G
NG_009029.2:g.7378A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*409-32A>G	ENSP00000509954.1:n.*409-32A>G
ENST00000378842.8:c.821-32A>G MANE Select	ENSP00000368119.4:n.821-32A>G
ENST00000378842.7:c.821-32A>G	ENSP00000368119.3:n.821-32A>G
ENST00000450095.6:c.494-32A>G	ENSP00000401956.2:n.494-32A>G
ENST00000488412.2:n.45A>G
ENST00000489643.6:n.901-32A>G
ENST00000554085.5:c.*565-32A>G	ENSP00000450419.1:n.*565-32A>G
ENST00000554550.5:c.*441-32A>G	ENSP00000451435.1:n.*441-32A>G
ENST00000554638.5:n.1293-32A>G
ENST00000555020.5:n.1282-32A>G
ENST00000555086.5:n.896A>G
ENST00000555754.1:n.237A>G
ENST00000556278.1:c.432+510A>G	ENSP00000451792.1:n.432+510A>G
ENST00000557706.5:n.1396-32A>G
NM_000155.3:c.821-32A>G	NP_000146.2:n.821-32A>G
NM_001258332.1:c.494-32A>G	NP_001245261.1:n.494-32A>G
NM_000155.4:c.821-32A>G MANE Select	NP_000146.2:n.821-32A>G
NM_001258332.2:c.494-32A>G	NP_001245261.1:n.494-32A>G