Canonical Allele Identifier: CA1845637648

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647977C= , CM000671.2:g.34647977C=	GRCh38
NC_000009.11:g.34647974C= , CM000671.1:g.34647974C=	GRCh37
NC_000009.10:g.34637974C=	NCBI36
NG_009029.1:g.6340C=
NG_028966.1:g.793C=
NG_009029.2:g.6389C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*95+16C=	ENSP00000509954.1:n.*95+16C=
ENST00000378842.8:c.507+16C= MANE Select	ENSP00000368119.4:n.507+16C=
ENST00000378842.7:c.507+16C=	ENSP00000368119.3:n.507+16C=
ENST00000450095.6:c.180+16C=	ENSP00000401956.2:n.180+16C=
ENST00000465543.6:n.846+16C=
ENST00000472111.5:n.763+16C=
ENST00000473506.6:c.*95+16C=	ENSP00000432839.2:n.*95+16C=
ENST00000473529.5:n.643+16C=
ENST00000485531.1:n.964C=
ENST00000487381.5:n.892+16C=
ENST00000489643.6:n.283-138C=
ENST00000554085.5:c.*251+16C=	ENSP00000450419.1:n.*251+16C=
ENST00000554139.5:n.686+16C=
ENST00000554550.5:c.*127+16C=	ENSP00000451435.1:n.*127+16C=
ENST00000554638.5:n.979+16C=
ENST00000554897.5:c.*127+16C=	ENSP00000450942.1:n.*127+16C=
ENST00000554944.5:n.719C=
ENST00000555020.5:n.663+16C=
ENST00000555086.5:n.511+16C=
ENST00000555214.5:n.262-71C=
ENST00000556244.1:c.494+16C=
ENST00000556278.1:c.253-138C=	ENSP00000451792.1:n.253-138C=
ENST00000556494.5:n.628+16C=
ENST00000557706.5:n.1069+16C=
NM_000155.3:c.507+16C=	NP_000146.2:n.507+16C=
NM_001258332.1:c.180+16C=	NP_001245261.1:n.180+16C=
NM_000155.4:c.507+16C= MANE Select	NP_000146.2:n.507+16C=
NM_001258332.2:c.180+16C=	NP_001245261.1:n.180+16C=