Canonical Allele Identifier: CA1845639979

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648877C= , CM000671.2:g.34648877C=	GRCh38
NC_000009.11:g.34648874C= , CM000671.1:g.34648874C=	GRCh37
NC_000009.10:g.34638874C=	NCBI36
NG_009029.1:g.7240C=
NG_028966.1:g.1693C=
NG_009029.2:g.7289C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*391C=	ENSP00000509954.1:n.*391C=
ENST00000378842.8:c.803C= MANE Select	ENSP00000368119.4:p.Thr268=
ENST00000378842.7:c.803C=	ENSP00000368119.3:p.Thr268=
ENST00000450095.6:c.476C=	ENSP00000401956.2:p.Thr159=
ENST00000473506.6:c.*391C=	ENSP00000432839.2:n.*391C=
ENST00000489643.6:n.883C=
ENST00000554085.5:c.*547C=	ENSP00000450419.1:n.*547C=
ENST00000554550.5:c.*423C=	ENSP00000451435.1:n.*423C=
ENST00000554638.5:n.1275C=
ENST00000555020.5:n.1264C=
ENST00000555086.5:n.807C=
ENST00000555754.1:n.148C=
ENST00000556244.1:c.790C=
ENST00000556278.1:c.432+421C=	ENSP00000451792.1:n.432+421C=
ENST00000557706.5:n.1365C=
NM_000155.3:c.803C=	NP_000146.2:p.Thr268=
NM_001258332.1:c.476C=	NP_001245261.1:p.Thr159=
NM_000155.4:c.803C= MANE Select	NP_000146.2:p.Thr268=
NM_001258332.2:c.476C=	NP_001245261.1:p.Thr159=