Canonical Allele Identifier: CA1845640477

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649051A= , CM000671.2:g.34649051A=	GRCh38
NC_000009.11:g.34649048A= , CM000671.1:g.34649048A=	GRCh37
NC_000009.10:g.34639048A=	NCBI36
NG_009029.1:g.7414A=
NG_028966.1:g.1867A=
NG_009029.2:g.7463A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*462A=	ENSP00000509954.1:n.*462A=
ENST00000378842.8:c.874A= MANE Select	ENSP00000368119.4:p.Thr292=
ENST00000378842.7:c.874A=	ENSP00000368119.3:p.Thr292=
ENST00000450095.6:c.547A=	ENSP00000401956.2:p.Thr183=
ENST00000488412.2:n.130A=
ENST00000489643.6:n.954A=
ENST00000554550.5:c.*494A=	ENSP00000451435.1:n.*494A=
ENST00000554638.5:n.1346A=
ENST00000555020.5:n.1335A=
ENST00000555086.5:n.981A=
ENST00000555754.1:n.322A=
ENST00000556278.1:c.432+595A=	ENSP00000451792.1:n.432+595A=
ENST00000557706.5:n.1449A=
NM_000155.3:c.874A=	NP_000146.2:p.Thr292=
NM_001258332.1:c.547A=	NP_001245261.1:p.Thr183=
NM_000155.4:c.874A= MANE Select	NP_000146.2:p.Thr292=
NM_001258332.2:c.547A=	NP_001245261.1:p.Thr183=