Canonical Allele Identifier: CA1845638687

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648367C= , CM000671.2:g.34648367C=	GRCh38
NC_000009.11:g.34648364C= , CM000671.1:g.34648364C=	GRCh37
NC_000009.10:g.34638364C=	NCBI36
NG_009029.1:g.6730C=
NG_028966.1:g.1183C=
NG_009029.2:g.6779C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*186C=	ENSP00000509954.1:n.*186C=
ENST00000378842.8:c.598C= MANE Select	ENSP00000368119.4:p.Gln200=
ENST00000378842.7:c.598C=	ENSP00000368119.3:p.Gln200=
ENST00000450095.6:c.271C=	ENSP00000401956.2:p.Gln91=
ENST00000472111.5:n.854C=
ENST00000473506.6:c.*186C=	ENSP00000432839.2:n.*186C=
ENST00000473529.5:n.757C=
ENST00000485531.1:n.1192C=
ENST00000487381.5:n.983C=
ENST00000489643.6:n.373C=
ENST00000554085.5:c.*342C=	ENSP00000450419.1:n.*342C=
ENST00000554139.5:n.844C=
ENST00000554550.5:c.*218C=	ENSP00000451435.1:n.*218C=
ENST00000554638.5:n.1070C=
ENST00000554897.5:c.*285C=	ENSP00000450942.1:n.*285C=
ENST00000554944.5:n.947C=
ENST00000555020.5:n.754C=
ENST00000555086.5:n.602C=
ENST00000555214.5:n.419C=
ENST00000556244.1:c.585C=
ENST00000556278.1:c.343C=	ENSP00000451792.1:p.Gln115=
ENST00000556494.5:n.719C=
ENST00000557706.5:n.1160C=
NM_000155.3:c.598C=	NP_000146.2:p.Gln200=
NM_001258332.1:c.271C=	NP_001245261.1:p.Gln91=
NM_000155.4:c.598C= MANE Select	NP_000146.2:p.Gln200=
NM_001258332.2:c.271C=	NP_001245261.1:p.Gln91=