Canonical Allele Identifier: CA1845639871

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648856T= , CM000671.2:g.34648856T=	GRCh38
NC_000009.11:g.34648853T= , CM000671.1:g.34648853T=	GRCh37
NC_000009.10:g.34638853T=	NCBI36
NG_009029.1:g.7219T=
NG_028966.1:g.1672T=
NG_009029.2:g.7268T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*370T=	ENSP00000509954.1:n.*370T=
ENST00000378842.8:c.782T= MANE Select	ENSP00000368119.4:p.Val261=
ENST00000378842.7:c.782T=	ENSP00000368119.3:p.Val261=
ENST00000450095.6:c.455T=	ENSP00000401956.2:p.Val152=
ENST00000473506.6:c.*370T=	ENSP00000432839.2:n.*370T=
ENST00000489643.6:n.862T=
ENST00000554085.5:c.*526T=	ENSP00000450419.1:n.*526T=
ENST00000554550.5:c.*402T=	ENSP00000451435.1:n.*402T=
ENST00000554638.5:n.1254T=
ENST00000555020.5:n.1243T=
ENST00000555086.5:n.786T=
ENST00000555754.1:n.127T=
ENST00000556244.1:c.769T=
ENST00000556278.1:c.432+400T=	ENSP00000451792.1:n.432+400T=
ENST00000557706.5:n.1344T=
NM_000155.3:c.782T=	NP_000146.2:p.Val261=
NM_001258332.1:c.455T=	NP_001245261.1:p.Val152=
NM_000155.4:c.782T= MANE Select	NP_000146.2:p.Val261=
NM_001258332.2:c.455T=	NP_001245261.1:p.Val152=