Canonical Allele Identifier: CA464401871

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648123C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648126C>T , CM000671.2:g.34648126C>T	GRCh38
NC_000009.11:g.34648123C>T , CM000671.1:g.34648123C>T	GRCh37
NC_000009.10:g.34638123C>T	NCBI36
NG_009029.1:g.6489C>T
NG_028966.1:g.942C>T
NG_009029.2:g.6538C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*107C>T	ENSP00000509954.1:n.*107C>T
ENST00000378842.8:c.519C>T MANE Select	ENSP00000368119.4:p.Asn173=
ENST00000378842.7:c.519C>T	ENSP00000368119.3:p.Asn173=
ENST00000450095.6:c.192C>T	ENSP00000401956.2:p.Asn64=
ENST00000465543.6:n.858C>T
ENST00000472111.5:n.775C>T
ENST00000473506.6:c.*107C>T	ENSP00000432839.2:n.*107C>T
ENST00000473529.5:n.678C>T
ENST00000485531.1:n.1113C>T
ENST00000487381.5:n.904C>T
ENST00000489643.6:n.294C>T
ENST00000554085.5:c.*263C>T	ENSP00000450419.1:n.*263C>T
ENST00000554139.5:n.765C>T
ENST00000554550.5:c.*139C>T	ENSP00000451435.1:n.*139C>T
ENST00000554638.5:n.991C>T
ENST00000554897.5:c.*206C>T	ENSP00000450942.1:n.*206C>T
ENST00000554944.5:n.868C>T
ENST00000555020.5:n.675C>T
ENST00000555086.5:n.523C>T
ENST00000555214.5:n.340C>T
ENST00000556244.1:c.506C>T
ENST00000556278.1:c.264C>T	ENSP00000451792.1:p.Asn88=
ENST00000556494.5:n.640C>T
ENST00000557706.5:n.1081C>T
NM_000155.3:c.519C>T	NP_000146.2:p.Asn173=
NM_001258332.1:c.192C>T	NP_001245261.1:p.Asn64=
NM_000155.4:c.519C>T MANE Select	NP_000146.2:p.Asn173=
NM_001258332.2:c.192C>T	NP_001245261.1:p.Asn64=