Canonical Allele Identifier: CA1845635758

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647237G= , CM000671.2:g.34647237G=	GRCh38
NC_000009.11:g.34647234G= , CM000671.1:g.34647234G=	GRCh37
NC_000009.10:g.34637234G=	NCBI36
NG_009029.1:g.5600G=
NG_028966.1:g.53G=
NG_009029.2:g.5649G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.231G=	ENSP00000509954.1:p.Gly77=
ENST00000378842.8:c.231G= MANE Select	ENSP00000368119.4:p.Gly77=
ENST00000378842.7:c.231G=	ENSP00000368119.3:p.Gly77=
ENST00000450095.6:c.29G=	ENSP00000401956.2:p.Gly10=
ENST00000465543.6:n.570G=
ENST00000468099.2:n.271G=
ENST00000472111.5:n.272G=
ENST00000473506.6:c.231G=	ENSP00000432839.2:p.Gly77=
ENST00000473529.5:n.278G=
ENST00000485531.1:n.224G=
ENST00000487381.5:n.257G=
ENST00000489643.6:n.261G=
ENST00000554085.5:c.231G=	ENSP00000450419.1:p.Gly77=
ENST00000554139.5:n.284G=
ENST00000554330.5:n.228G=
ENST00000554550.5:c.231G=	ENSP00000451435.1:p.Gly77=
ENST00000554638.5:n.255G=
ENST00000554897.5:c.231G=	ENSP00000450942.1:p.Gly77=
ENST00000554944.5:n.261G=
ENST00000555020.5:n.261G=
ENST00000555086.5:n.235G=
ENST00000555214.5:n.240G=
ENST00000556157.1:n.338G=
ENST00000556244.1:c.115G=
ENST00000556278.1:c.231G=	ENSP00000451792.1:p.Gly77=
ENST00000556403.5:n.244G=
ENST00000556494.5:n.263G=
ENST00000557541.5:n.424G=
ENST00000557706.5:n.345G=
NM_000155.3:c.231G=	NP_000146.2:p.Gly77=
NM_001258332.1:c.29G=	NP_001245261.1:p.Gly10=
NM_000155.4:c.231G= MANE Select	NP_000146.2:p.Gly77=
NM_001258332.2:c.29G=	NP_001245261.1:p.Gly10=