Canonical Allele Identifier: CA1845639289

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648616T= , CM000671.2:g.34648616T=	GRCh38
NC_000009.11:g.34648613T= , CM000671.1:g.34648613T=	GRCh37
NC_000009.10:g.34638613T=	NCBI36
NG_009029.1:g.6979T=
NG_028966.1:g.1432T=
NG_009029.2:g.7028T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*276-146T=	ENSP00000509954.1:n.*276-146T=
ENST00000378842.8:c.688-146T= MANE Select	ENSP00000368119.4:n.688-146T=
ENST00000378842.7:c.688-146T=	ENSP00000368119.3:n.688-146T=
ENST00000450095.6:c.361-146T=	ENSP00000401956.2:n.361-146T=
ENST00000473506.6:c.*276-146T=	ENSP00000432839.2:n.*276-146T=
ENST00000473529.5:n.847-146T=
ENST00000487381.5:n.1232T=
ENST00000489643.6:n.622T=
ENST00000554085.5:c.*432-146T=	ENSP00000450419.1:n.*432-146T=
ENST00000554550.5:c.*308-146T=	ENSP00000451435.1:n.*308-146T=
ENST00000554638.5:n.1160-146T=
ENST00000555020.5:n.1003T=
ENST00000555086.5:n.692-146T=
ENST00000555214.5:n.668T=
ENST00000555754.1:n.33-146T=
ENST00000556244.1:c.675-146T=
ENST00000556278.1:c.432+160T=	ENSP00000451792.1:n.432+160T=
ENST00000557706.5:n.1250-146T=
NM_000155.3:c.688-146T=	NP_000146.2:n.688-146T=
NM_001258332.1:c.361-146T=	NP_001245261.1:n.361-146T=
NM_000155.4:c.688-146T= MANE Select	NP_000146.2:n.688-146T=
NM_001258332.2:c.361-146T=	NP_001245261.1:n.361-146T=