Canonical Allele Identifier: CA1845636782

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647758C= , CM000671.2:g.34647758C=	GRCh38
NC_000009.11:g.34647755C= , CM000671.1:g.34647755C=	GRCh37
NC_000009.10:g.34637755C=	NCBI36
NG_009029.1:g.6121C=
NG_028966.1:g.574C=
NG_009029.2:g.6170C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.329-74C=	ENSP00000509954.1:n.329-74C=
ENST00000378842.8:c.377+53C= MANE Select	ENSP00000368119.4:n.377+53C=
ENST00000378842.7:c.377+53C=	ENSP00000368119.3:n.377+53C=
ENST00000450095.6:c.51-74C=	ENSP00000401956.2:n.51-74C=
ENST00000465543.6:n.716+53C=
ENST00000472111.5:n.560C=
ENST00000473506.6:c.328+53C=	ENSP00000432839.2:n.328+53C=
ENST00000473529.5:n.513+53C=
ENST00000485531.1:n.745C=
ENST00000487381.5:n.689C=
ENST00000489643.6:n.283-357C=
ENST00000554085.5:c.*121+53C=	ENSP00000450419.1:n.*121+53C=
ENST00000554139.5:n.483C=
ENST00000554330.5:n.467C=
ENST00000554550.5:c.253-74C=	ENSP00000451435.1:n.253-74C=
ENST00000554638.5:n.776C=
ENST00000554897.5:c.253-74C=	ENSP00000450942.1:n.253-74C=
ENST00000554944.5:n.500C=
ENST00000555020.5:n.460C=
ENST00000555086.5:n.381+53C=
ENST00000555214.5:n.262-290C=
ENST00000556157.1:n.554C=
ENST00000556244.1:c.364+53C=
ENST00000556278.1:c.253-357C=	ENSP00000451792.1:n.253-357C=
ENST00000556403.5:n.532C=
ENST00000556494.5:n.498+53C=
ENST00000557541.5:n.521+53C=
ENST00000557706.5:n.866C=
NM_000155.3:c.377+53C=	NP_000146.2:n.377+53C=
NM_001258332.1:c.51-74C=	NP_001245261.1:n.51-74C=
NM_000155.4:c.377+53C= MANE Select	NP_000146.2:n.377+53C=
NM_001258332.2:c.51-74C=	NP_001245261.1:n.51-74C=