Canonical Allele Identifier: CA1845636601

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647696G= , CM000671.2:g.34647696G=	GRCh38
NC_000009.11:g.34647693G= , CM000671.1:g.34647693G=	GRCh37
NC_000009.10:g.34637693G=	NCBI36
NG_009029.1:g.6059G=
NG_028966.1:g.512G=
NG_009029.2:g.6108G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+129G=	ENSP00000509954.1:n.328+129G=
ENST00000378842.8:c.368G= MANE Select	ENSP00000368119.4:p.Arg123=
ENST00000378842.7:c.368G=	ENSP00000368119.3:p.Arg123=
ENST00000450095.6:c.51-136G=	ENSP00000401956.2:n.51-136G=
ENST00000465543.6:n.707G=
ENST00000472111.5:n.498G=
ENST00000473506.6:c.319G=	ENSP00000432839.2:p.Glu107=
ENST00000473529.5:n.504G=
ENST00000485531.1:n.683G=
ENST00000487381.5:n.627G=
ENST00000489643.6:n.283-419G=
ENST00000554085.5:c.*112G=	ENSP00000450419.1:n.*112G=
ENST00000554139.5:n.421G=
ENST00000554330.5:n.405G=
ENST00000554550.5:c.253-136G=	ENSP00000451435.1:n.253-136G=
ENST00000554638.5:n.714G=
ENST00000554897.5:c.253-136G=	ENSP00000450942.1:n.253-136G=
ENST00000554944.5:n.438G=
ENST00000555020.5:n.398G=
ENST00000555086.5:n.372G=
ENST00000555214.5:n.262-352G=
ENST00000556157.1:n.492G=
ENST00000556244.1:c.355G=
ENST00000556278.1:c.253-419G=	ENSP00000451792.1:n.253-419G=
ENST00000556403.5:n.470G=
ENST00000556494.5:n.489G=
ENST00000557541.5:n.512G=
ENST00000557706.5:n.804G=
NM_000155.3:c.368G=	NP_000146.2:p.Arg123=
NM_001258332.1:c.51-136G=	NP_001245261.1:n.51-136G=
NM_000155.4:c.368G= MANE Select	NP_000146.2:p.Arg123=
NM_001258332.2:c.51-136G=	NP_001245261.1:n.51-136G=