Canonical Allele Identifier: CA1845635236

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647075C= , CM000671.2:g.34647075C=	GRCh38
NC_000009.11:g.34647072C= , CM000671.1:g.34647072C=	GRCh37
NC_000009.10:g.34637072C=	NCBI36
NG_009029.1:g.5438C=
NG_009029.2:g.5487C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.83-14C=	ENSP00000509954.1:n.83-14C=
ENST00000378842.8:c.83-14C= MANE Select	ENSP00000368119.4:n.83-14C=
ENST00000378842.7:c.83-14C=	ENSP00000368119.3:n.83-14C=
ENST00000450095.6:c.-120-14C=	ENSP00000401956.2:n.-120-14C=
ENST00000465543.6:n.408C=
ENST00000468099.2:n.155-46C=
ENST00000472111.5:n.124-14C=
ENST00000473506.6:c.83-14C=	ENSP00000432839.2:n.83-14C=
ENST00000473529.5:n.130-14C=
ENST00000485531.1:n.76-14C=
ENST00000487381.5:n.109-14C=
ENST00000489643.6:n.113-14C=
ENST00000554085.5:c.83-14C=	ENSP00000450419.1:n.83-14C=
ENST00000554139.5:n.136-14C=
ENST00000554330.5:n.80-14C=
ENST00000554550.5:c.83-14C=	ENSP00000451435.1:n.83-14C=
ENST00000554638.5:n.107-14C=
ENST00000554897.5:c.83-14C=	ENSP00000450942.1:n.83-14C=
ENST00000554944.5:n.113-14C=
ENST00000555020.5:n.113-14C=
ENST00000555086.5:n.87-14C=
ENST00000555214.5:n.92-14C=
ENST00000556157.1:n.176C=
ENST00000556278.1:c.83-14C=	ENSP00000451792.1:n.83-14C=
ENST00000556403.5:n.96-14C=
ENST00000556494.5:n.115-14C=
ENST00000557541.5:n.276-14C=
ENST00000557706.5:n.183C=
ENST00000605275.1:n.607C=
NM_000155.3:c.83-14C=	NP_000146.2:n.83-14C=
NM_001258332.1:c.-120-14C=	NP_001245261.1:n.-120-14C=
NM_000155.4:c.83-14C= MANE Select	NP_000146.2:n.83-14C=
NM_001258332.2:c.-120-14C=	NP_001245261.1:n.-120-14C=