Canonical Allele Identifier: CA1845636920

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647833A= , CM000671.2:g.34647833A=	GRCh38
NC_000009.11:g.34647830A= , CM000671.1:g.34647830A=	GRCh37
NC_000009.10:g.34637830A=	NCBI36
NG_009029.1:g.6196A=
NG_028966.1:g.649A=
NG_009029.2:g.6245A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000155.4:c.379A= MANE Select	NP_000146.2:p.Lys127=
ENST00000378842.8:c.379A= MANE Select	ENSP00000368119.4:p.Lys127=
NM_000155.3:c.379A=	NP_000146.2:p.Lys127=
NM_001258332.1:c.52A=	NP_001245261.1:p.Lys18=
NM_001258332.2:c.52A=	NP_001245261.1:p.Lys18=
ENST00000378842.7:c.379A=	ENSP00000368119.3:p.Lys127=
ENST00000450095.6:c.52A=	ENSP00000401956.2:p.Lys18=
ENST00000465543.6:n.718A=
ENST00000472111.5:n.635A=
ENST00000473506.6:c.330A=	ENSP00000432839.2:p.Val110=
ENST00000473529.5:n.515A=
ENST00000485531.1:n.820A=
ENST00000487381.5:n.764A=
ENST00000489643.6:n.283-282A=
ENST00000554085.5:c.*123A=	ENSP00000450419.1:n.*123A=
ENST00000554139.5:n.558A=
ENST00000554330.5:n.542A=
ENST00000554550.5:c.254A=	ENSP00000451435.1:p.Ter85=
ENST00000554638.5:n.851A=
ENST00000554897.5:c.254A=	ENSP00000450942.1:p.Ter85=
ENST00000554944.5:n.575A=
ENST00000555020.5:n.535A=
ENST00000555086.5:n.383A=
ENST00000555214.5:n.262-215A=
ENST00000556244.1:c.366A=
ENST00000556278.1:c.253-282A=	ENSP00000451792.1:n.253-282A=
ENST00000556494.5:n.500A=
ENST00000557541.5:n.523A=
ENST00000557706.5:n.941A=
ENST00000691183.1:c.330A=	ENSP00000509954.1:p.Val110=