Canonical Allele Identifier: CA2579371300

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648331C>T , CM000671.2:g.34648331C>T	GRCh38
NC_000009.11:g.34648328C>T , CM000671.1:g.34648328C>T	GRCh37
NC_000009.10:g.34638328C>T	NCBI36
NG_009029.1:g.6694C>T
NG_028966.1:g.1147C>T
NG_009029.2:g.6743C>T

Transcript Alleles

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