Canonical Allele Identifier: CA464595745

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647557C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647560C>T , CM000671.2:g.34647560C>T	GRCh38
NC_000009.11:g.34647557C>T , CM000671.1:g.34647557C>T	GRCh37
NC_000009.10:g.34637557C>T	NCBI36
NG_009029.1:g.5923C>T
NG_028966.1:g.376C>T
NG_009029.2:g.5972C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.321C>T	ENSP00000509954.1:p.Pro107=
ENST00000378842.8:c.321C>T MANE Select	ENSP00000368119.4:p.Pro107=
ENST00000378842.7:c.321C>T	ENSP00000368119.3:p.Pro107=
ENST00000450095.6:c.51-272C>T	ENSP00000401956.2:n.51-272C>T
ENST00000465543.6:n.660C>T
ENST00000472111.5:n.362C>T
ENST00000473506.6:c.272C>T	ENSP00000432839.2:p.Pro91Leu
ENST00000473529.5:n.368C>T
ENST00000485531.1:n.547C>T
ENST00000487381.5:n.580C>T
ENST00000489643.6:n.282+302C>T
ENST00000554085.5:c.*65C>T	ENSP00000450419.1:n.*65C>T
ENST00000554139.5:n.374C>T
ENST00000554330.5:n.269C>T
ENST00000554550.5:c.253-272C>T	ENSP00000451435.1:n.253-272C>T
ENST00000554638.5:n.578C>T
ENST00000554897.5:c.253-272C>T	ENSP00000450942.1:n.253-272C>T
ENST00000554944.5:n.302C>T
ENST00000555020.5:n.351C>T
ENST00000555086.5:n.325C>T
ENST00000555214.5:n.261+302C>T
ENST00000556157.1:n.445C>T
ENST00000556244.1:c.308C>T
ENST00000556278.1:c.252+302C>T	ENSP00000451792.1:n.252+302C>T
ENST00000556403.5:n.334C>T
ENST00000556494.5:n.353C>T
ENST00000557541.5:n.465C>T
ENST00000557706.5:n.668C>T
NM_000155.3:c.321C>T	NP_000146.2:p.Pro107=
NM_001258332.1:c.51-272C>T	NP_001245261.1:n.51-272C>T
NM_000155.4:c.321C>T MANE Select	NP_000146.2:p.Pro107=
NM_001258332.2:c.51-272C>T	NP_001245261.1:n.51-272C>T