Canonical Allele Identifier: CA464595805

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647201C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647204C>T , CM000671.2:g.34647204C>T	GRCh38
NC_000009.11:g.34647201C>T , CM000671.1:g.34647201C>T	GRCh37
NC_000009.10:g.34637201C>T	NCBI36
NG_009029.1:g.5567C>T
NG_028966.1:g.20C>T
NG_009029.2:g.5616C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.198C>T	ENSP00000509954.1:p.Pro66=
ENST00000378842.8:c.198C>T MANE Select	ENSP00000368119.4:p.Pro66=
ENST00000378842.7:c.198C>T	ENSP00000368119.3:p.Pro66=
ENST00000450095.6:c.-5C>T	ENSP00000401956.2:n.-5C>T
ENST00000465543.6:n.537C>T
ENST00000468099.2:n.238C>T
ENST00000472111.5:n.239C>T
ENST00000473506.6:c.198C>T	ENSP00000432839.2:p.Pro66=
ENST00000473529.5:n.245C>T
ENST00000485531.1:n.191C>T
ENST00000487381.5:n.224C>T
ENST00000489643.6:n.228C>T
ENST00000554085.5:c.198C>T	ENSP00000450419.1:p.Pro66=
ENST00000554139.5:n.251C>T
ENST00000554330.5:n.195C>T
ENST00000554550.5:c.198C>T	ENSP00000451435.1:p.Pro66=
ENST00000554638.5:n.222C>T
ENST00000554897.5:c.198C>T	ENSP00000450942.1:p.Pro66=
ENST00000554944.5:n.228C>T
ENST00000555020.5:n.228C>T
ENST00000555086.5:n.202C>T
ENST00000555214.5:n.207C>T
ENST00000556157.1:n.305C>T
ENST00000556244.1:c.82C>T
ENST00000556278.1:c.198C>T	ENSP00000451792.1:p.Pro66=
ENST00000556403.5:n.211C>T
ENST00000556494.5:n.230C>T
ENST00000557541.5:n.391C>T
ENST00000557706.5:n.312C>T
NM_000155.3:c.198C>T	NP_000146.2:p.Pro66=
NM_001258332.1:c.-5C>T	NP_001245261.1:n.-5C>T
NM_000155.4:c.198C>T MANE Select	NP_000146.2:p.Pro66=
NM_001258332.2:c.-5C>T	NP_001245261.1:n.-5C>T