Canonical Allele Identifier: CA2579371296

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648284C>G , CM000671.2:g.34648284C>G	GRCh38
NC_000009.11:g.34648281C>G , CM000671.1:g.34648281C>G	GRCh37
NC_000009.10:g.34638281C>G	NCBI36
NG_009029.1:g.6647C>G
NG_028966.1:g.1100C>G
NG_009029.2:g.6696C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*153-50C>G	ENSP00000509954.1:n.*153-50C>G
ENST00000378842.8:c.565-50C>G MANE Select	ENSP00000368119.4:n.565-50C>G
ENST00000378842.7:c.565-50C>G	ENSP00000368119.3:n.565-50C>G
ENST00000450095.6:c.238-50C>G	ENSP00000401956.2:n.238-50C>G
ENST00000472111.5:n.821-50C>G
ENST00000473506.6:c.*153-50C>G	ENSP00000432839.2:n.*153-50C>G
ENST00000473529.5:n.724-50C>G
ENST00000485531.1:n.1159-50C>G
ENST00000487381.5:n.950-50C>G
ENST00000489643.6:n.340-50C>G
ENST00000554085.5:c.*309-50C>G	ENSP00000450419.1:n.*309-50C>G
ENST00000554139.5:n.811-50C>G
ENST00000554550.5:c.*185-50C>G	ENSP00000451435.1:n.*185-50C>G
ENST00000554638.5:n.1037-50C>G
ENST00000554897.5:c.*252-50C>G	ENSP00000450942.1:n.*252-50C>G
ENST00000554944.5:n.914-50C>G
ENST00000555020.5:n.721-50C>G
ENST00000555086.5:n.569-50C>G
ENST00000555214.5:n.386-50C>G
ENST00000556244.1:c.552-50C>G
ENST00000556278.1:c.310-50C>G	ENSP00000451792.1:n.310-50C>G
ENST00000556494.5:n.686-50C>G
ENST00000557706.5:n.1127-50C>G
NM_000155.3:c.565-50C>G	NP_000146.2:n.565-50C>G
NM_001258332.1:c.238-50C>G	NP_001245261.1:n.238-50C>G
NM_000155.4:c.565-50C>G MANE Select	NP_000146.2:n.565-50C>G
NM_001258332.2:c.238-50C>G	NP_001245261.1:n.238-50C>G