Canonical Allele Identifier: CA1845638650

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648363T= , CM000671.2:g.34648363T=	GRCh38
NC_000009.11:g.34648360T= , CM000671.1:g.34648360T=	GRCh37
NC_000009.10:g.34638360T=	NCBI36
NG_009029.1:g.6726T=
NG_028966.1:g.1179T=
NG_009029.2:g.6775T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*182T=	ENSP00000509954.1:n.*182T=
ENST00000378842.8:c.594T= MANE Select	ENSP00000368119.4:p.Ile198=
ENST00000378842.7:c.594T=	ENSP00000368119.3:p.Ile198=
ENST00000450095.6:c.267T=	ENSP00000401956.2:p.Ile89=
ENST00000472111.5:n.850T=
ENST00000473506.6:c.*182T=	ENSP00000432839.2:n.*182T=
ENST00000473529.5:n.753T=
ENST00000485531.1:n.1188T=
ENST00000487381.5:n.979T=
ENST00000489643.6:n.369T=
ENST00000554085.5:c.*338T=	ENSP00000450419.1:n.*338T=
ENST00000554139.5:n.840T=
ENST00000554550.5:c.*214T=	ENSP00000451435.1:n.*214T=
ENST00000554638.5:n.1066T=
ENST00000554897.5:c.*281T=	ENSP00000450942.1:n.*281T=
ENST00000554944.5:n.943T=
ENST00000555020.5:n.750T=
ENST00000555086.5:n.598T=
ENST00000555214.5:n.415T=
ENST00000556244.1:c.581T=
ENST00000556278.1:c.339T=	ENSP00000451792.1:p.Ile113=
ENST00000556494.5:n.715T=
ENST00000557706.5:n.1156T=
NM_000155.3:c.594T=	NP_000146.2:p.Ile198=
NM_001258332.1:c.267T=	NP_001245261.1:p.Ile89=
NM_000155.4:c.594T= MANE Select	NP_000146.2:p.Ile198=
NM_001258332.2:c.267T=	NP_001245261.1:p.Ile89=