Canonical Allele Identifier: CA1845639917

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648864_34648866delinsCTA , CM000671.2:g.34648864_34648866delinsCTA	GRCh38
NC_000009.11:g.34648861_34648863delinsCTA , CM000671.1:g.34648861_34648863delinsCTA	GRCh37
NC_000009.10:g.34638861_34638863delinsCTA	NCBI36
NG_009029.1:g.7227_7229delinsCTA
NG_028966.1:g.1680_1682delinsCTA
NG_009029.2:g.7276_7278delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*378_*380delinsCTA	ENSP00000509954.1:n.*378_*380delinsCTA
ENST00000378842.8:c.790_792delinsCTA MANE Select	ENSP00000368119.4:p.Leu264=
ENST00000378842.7:c.790_792delinsCTA	ENSP00000368119.3:p.Leu264=
ENST00000450095.6:c.463_465delinsCTA	ENSP00000401956.2:p.Leu155=
ENST00000473506.6:c.*378_*380delinsCTA	ENSP00000432839.2:n.*378_*380delinsCTA
ENST00000489643.6:n.870_872delinsCTA
ENST00000554085.5:c.*534_*536delinsCTA	ENSP00000450419.1:n.*534_*536delinsCTA
ENST00000554550.5:c.*410_*412delinsCTA	ENSP00000451435.1:n.*410_*412delinsCTA
ENST00000554638.5:n.1262_1264delinsCTA
ENST00000555020.5:n.1251_1253delinsCTA
ENST00000555086.5:n.794_796delinsCTA
ENST00000555754.1:n.135_137delinsCTA
ENST00000556244.1:c.777_779delinsCTA
ENST00000556278.1:c.432+408_432+410delinsCTA	ENSP00000451792.1:n.432+408_432+410delinsCTA
ENST00000557706.5:n.1352_1354delinsCTA
NM_000155.3:c.790_792delinsCTA	NP_000146.2:p.Leu264=
NM_001258332.1:c.463_465delinsCTA	NP_001245261.1:p.Leu155=
NM_000155.4:c.790_792delinsCTA MANE Select	NP_000146.2:p.Leu264=
NM_001258332.2:c.463_465delinsCTA	NP_001245261.1:p.Leu155=