Canonical Allele Identifier: CA1845636811

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647779G= , CM000671.2:g.34647779G=	GRCh38
NC_000009.11:g.34647776G= , CM000671.1:g.34647776G=	GRCh37
NC_000009.10:g.34637776G=	NCBI36
NG_009029.1:g.6142G=
NG_028966.1:g.595G=
NG_009029.2:g.6191G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.329-53G=	ENSP00000509954.1:n.329-53G=
ENST00000378842.8:c.378-53G= MANE Select	ENSP00000368119.4:n.378-53G=
ENST00000378842.7:c.378-53G=	ENSP00000368119.3:n.378-53G=
ENST00000450095.6:c.51-53G=	ENSP00000401956.2:n.51-53G=
ENST00000465543.6:n.717-53G=
ENST00000472111.5:n.581G=
ENST00000473506.6:c.329-53G=	ENSP00000432839.2:n.329-53G=
ENST00000473529.5:n.514-53G=
ENST00000485531.1:n.766G=
ENST00000487381.5:n.710G=
ENST00000489643.6:n.283-336G=
ENST00000554085.5:c.*122-53G=	ENSP00000450419.1:n.*122-53G=
ENST00000554139.5:n.504G=
ENST00000554330.5:n.488G=
ENST00000554550.5:c.253-53G=	ENSP00000451435.1:n.253-53G=
ENST00000554638.5:n.797G=
ENST00000554897.5:c.253-53G=	ENSP00000450942.1:n.253-53G=
ENST00000554944.5:n.521G=
ENST00000555020.5:n.481G=
ENST00000555086.5:n.382-53G=
ENST00000555214.5:n.262-269G=
ENST00000556244.1:c.365-53G=
ENST00000556278.1:c.253-336G=	ENSP00000451792.1:n.253-336G=
ENST00000556403.5:n.553G=
ENST00000556494.5:n.499-53G=
ENST00000557541.5:n.522-53G=
ENST00000557706.5:n.887G=
NM_000155.3:c.378-53G=	NP_000146.2:n.378-53G=
NM_001258332.1:c.51-53G=	NP_001245261.1:n.51-53G=
NM_000155.4:c.378-53G= MANE Select	NP_000146.2:n.378-53G=
NM_001258332.2:c.51-53G=	NP_001245261.1:n.51-53G=