Canonical Allele Identifier: CA464595653

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647102C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647105C>T , CM000671.2:g.34647105C>T	GRCh38
NC_000009.11:g.34647102C>T , CM000671.1:g.34647102C>T	GRCh37
NC_000009.10:g.34637102C>T	NCBI36
NG_009029.1:g.5468C>T
NG_009029.2:g.5517C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.99C>T	ENSP00000509954.1:p.Arg33=
ENST00000378842.8:c.99C>T MANE Select	ENSP00000368119.4:p.Arg33=
ENST00000378842.7:c.99C>T	ENSP00000368119.3:p.Arg33=
ENST00000450095.6:c.-104C>T	ENSP00000401956.2:n.-104C>T
ENST00000465543.6:n.438C>T
ENST00000468099.2:n.155-16C>T
ENST00000472111.5:n.140C>T
ENST00000473506.6:c.99C>T	ENSP00000432839.2:p.Arg33=
ENST00000473529.5:n.146C>T
ENST00000485531.1:n.92C>T
ENST00000487381.5:n.125C>T
ENST00000489643.6:n.129C>T
ENST00000554085.5:c.99C>T	ENSP00000450419.1:p.Arg33=
ENST00000554139.5:n.152C>T
ENST00000554330.5:n.96C>T
ENST00000554550.5:c.99C>T	ENSP00000451435.1:p.Arg33=
ENST00000554638.5:n.123C>T
ENST00000554897.5:c.99C>T	ENSP00000450942.1:p.Arg33=
ENST00000554944.5:n.129C>T
ENST00000555020.5:n.129C>T
ENST00000555086.5:n.103C>T
ENST00000555214.5:n.108C>T
ENST00000556157.1:n.206C>T
ENST00000556278.1:c.99C>T	ENSP00000451792.1:p.Arg33=
ENST00000556403.5:n.112C>T
ENST00000556494.5:n.131C>T
ENST00000557541.5:n.292C>T
ENST00000557706.5:n.213C>T
ENST00000605275.1:n.637C>T
NM_000155.3:c.99C>T	NP_000146.2:p.Arg33=
NM_001258332.1:c.-104C>T	NP_001245261.1:n.-104C>T
NM_000155.4:c.99C>T MANE Select	NP_000146.2:p.Arg33=
NM_001258332.2:c.-104C>T	NP_001245261.1:n.-104C>T