Canonical Allele Identifier: CA1845637765

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648032A= , CM000671.2:g.34648032A=	GRCh38
NC_000009.11:g.34648029A= , CM000671.1:g.34648029A=	GRCh37
NC_000009.10:g.34638029A=	NCBI36
NG_009029.1:g.6395A=
NG_028966.1:g.848A=
NG_009029.2:g.6444A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*95+71A=	ENSP00000509954.1:n.*95+71A=
ENST00000378842.8:c.507+71A= MANE Select	ENSP00000368119.4:n.507+71A=
ENST00000378842.7:c.507+71A=	ENSP00000368119.3:n.507+71A=
ENST00000450095.6:c.180+71A=	ENSP00000401956.2:n.180+71A=
ENST00000465543.6:n.846+71A=
ENST00000472111.5:n.763+71A=
ENST00000473506.6:c.*95+71A=	ENSP00000432839.2:n.*95+71A=
ENST00000473529.5:n.644-60A=
ENST00000485531.1:n.1019A=
ENST00000487381.5:n.892+71A=
ENST00000489643.6:n.283-83A=
ENST00000554085.5:c.*251+71A=	ENSP00000450419.1:n.*251+71A=
ENST00000554139.5:n.687-16A=
ENST00000554550.5:c.*127+71A=	ENSP00000451435.1:n.*127+71A=
ENST00000554638.5:n.979+71A=
ENST00000554897.5:c.*128-16A=	ENSP00000450942.1:n.*128-16A=
ENST00000554944.5:n.774A=
ENST00000555020.5:n.663+71A=
ENST00000555086.5:n.511+71A=
ENST00000555214.5:n.262-16A=
ENST00000556244.1:c.494+71A=
ENST00000556278.1:c.253-83A=	ENSP00000451792.1:n.253-83A=
ENST00000556494.5:n.628+71A=
ENST00000557706.5:n.1069+71A=
NM_000155.3:c.507+71A=	NP_000146.2:n.507+71A=
NM_001258332.1:c.180+71A=	NP_001245261.1:n.180+71A=
NM_000155.4:c.507+71A= MANE Select	NP_000146.2:n.507+71A=
NM_001258332.2:c.180+71A=	NP_001245261.1:n.180+71A=