Canonical Allele Identifier: CA1845636553

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647682A= , CM000671.2:g.34647682A=	GRCh38
NC_000009.11:g.34647679A= , CM000671.1:g.34647679A=	GRCh37
NC_000009.10:g.34637679A=	NCBI36
NG_009029.1:g.6045A=
NG_028966.1:g.498A=
NG_009029.2:g.6094A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+115A=	ENSP00000509954.1:n.328+115A=
ENST00000378842.8:c.354A= MANE Select	ENSP00000368119.4:p.Gln118=
ENST00000378842.7:c.354A=	ENSP00000368119.3:p.Gln118=
ENST00000450095.6:c.51-150A=	ENSP00000401956.2:n.51-150A=
ENST00000465543.6:n.693A=
ENST00000472111.5:n.484A=
ENST00000473506.6:c.305A=	ENSP00000432839.2:p.Lys102=
ENST00000473529.5:n.490A=
ENST00000485531.1:n.669A=
ENST00000487381.5:n.613A=
ENST00000489643.6:n.282+424A=
ENST00000554085.5:c.*98A=	ENSP00000450419.1:n.*98A=
ENST00000554139.5:n.407A=
ENST00000554330.5:n.391A=
ENST00000554550.5:c.253-150A=	ENSP00000451435.1:n.253-150A=
ENST00000554638.5:n.700A=
ENST00000554897.5:c.253-150A=	ENSP00000450942.1:n.253-150A=
ENST00000554944.5:n.424A=
ENST00000555020.5:n.384A=
ENST00000555086.5:n.358A=
ENST00000555214.5:n.262-366A=
ENST00000556157.1:n.478A=
ENST00000556244.1:c.341A=
ENST00000556278.1:c.252+424A=	ENSP00000451792.1:n.252+424A=
ENST00000556403.5:n.456A=
ENST00000556494.5:n.475A=
ENST00000557541.5:n.498A=
ENST00000557706.5:n.790A=
NM_000155.3:c.354A=	NP_000146.2:p.Gln118=
NM_001258332.1:c.51-150A=	NP_001245261.1:n.51-150A=
NM_000155.4:c.354A= MANE Select	NP_000146.2:p.Gln118=
NM_001258332.2:c.51-150A=	NP_001245261.1:n.51-150A=