Canonical Allele Identifier: CA913157561

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34646714dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646718dup , CM000671.2:g.34646718dup	GRCh38
NC_000009.11:g.34646715dup , CM000671.1:g.34646715dup	GRCh37
NC_000009.10:g.34636715dup	NCBI36
NG_009029.1:g.5081dup
NG_009029.2:g.5130dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.14dup	ENSP00000509954.1:p.Thr6AsnfsTer?
ENST00000378842.8:c.14dup MANE Select	ENSP00000368119.4:p.Thr6AsnfsTer?
ENST00000378842.7:c.14dup	ENSP00000368119.3:p.Thr6AsnfsTer?
ENST00000450095.6:c.-189dup	ENSP00000401956.2:n.-189dup
ENST00000465543.6:n.51dup
ENST00000468099.2:n.86dup
ENST00000472111.5:n.55dup
ENST00000473506.6:c.14dup	ENSP00000432839.2:p.Thr6AsnfsTer?
ENST00000473529.5:n.61dup
ENST00000487381.5:n.40dup
ENST00000489643.6:n.44dup
ENST00000554085.5:c.14dup	ENSP00000450419.1:p.Thr6AsnfsTer?
ENST00000554139.5:n.67dup
ENST00000554550.5:c.14dup	ENSP00000451435.1:p.Thr6AsnfsTer?
ENST00000554638.5:n.38dup
ENST00000554897.5:c.14dup	ENSP00000450942.1:p.Thr6AsnfsTer?
ENST00000554944.5:n.44dup
ENST00000555020.5:n.44dup
ENST00000555214.5:n.23dup
ENST00000556278.1:c.14dup	ENSP00000451792.1:p.Thr6AsnfsTer?
ENST00000557541.5:n.74dup
ENST00000605275.1:n.250dup
NM_000155.3:c.14dup	NP_000146.2:p.Thr6AsnfsTer?
NM_001258332.1:c.-189dup	NP_001245261.1:n.-189dup
NM_000155.4:c.14dup MANE Select	NP_000146.2:p.Thr6AsnfsTer?
NM_001258332.2:c.-189dup	NP_001245261.1:n.-189dup