Canonical Allele Identifier: CA1845637227

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647874A= , CM000671.2:g.34647874A=	GRCh38
NC_000009.11:g.34647871A= , CM000671.1:g.34647871A=	GRCh37
NC_000009.10:g.34637871A=	NCBI36
NG_009029.1:g.6237A=
NG_028966.1:g.690A=
NG_009029.2:g.6286A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*8A=	ENSP00000509954.1:n.*8A=
ENST00000378842.8:c.420A= MANE Select	ENSP00000368119.4:p.Pro140=
ENST00000378842.7:c.420A=	ENSP00000368119.3:p.Pro140=
ENST00000450095.6:c.93A=	ENSP00000401956.2:p.Pro31=
ENST00000465543.6:n.759A=
ENST00000472111.5:n.676A=
ENST00000473506.6:c.*8A=	ENSP00000432839.2:n.*8A=
ENST00000473529.5:n.556A=
ENST00000485531.1:n.861A=
ENST00000487381.5:n.805A=
ENST00000489643.6:n.283-241A=
ENST00000554085.5:c.*164A=	ENSP00000450419.1:n.*164A=
ENST00000554139.5:n.599A=
ENST00000554550.5:c.*40A=	ENSP00000451435.1:n.*40A=
ENST00000554638.5:n.892A=
ENST00000554897.5:c.*40A=	ENSP00000450942.1:n.*40A=
ENST00000554944.5:n.616A=
ENST00000555020.5:n.576A=
ENST00000555086.5:n.424A=
ENST00000555214.5:n.262-174A=
ENST00000556244.1:c.407A=
ENST00000556278.1:c.253-241A=	ENSP00000451792.1:n.253-241A=
ENST00000556494.5:n.541A=
ENST00000557541.5:n.564A=
ENST00000557706.5:n.982A=
NM_000155.3:c.420A=	NP_000146.2:p.Pro140=
NM_001258332.1:c.93A=	NP_001245261.1:p.Pro31=
NM_000155.4:c.420A= MANE Select	NP_000146.2:p.Pro140=
NM_001258332.2:c.93A=	NP_001245261.1:p.Pro31=