Canonical Allele Identifier: CA464595852

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647691T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647694T>A , CM000671.2:g.34647694T>A	GRCh38
NC_000009.11:g.34647691T>A , CM000671.1:g.34647691T>A	GRCh37
NC_000009.10:g.34637691T>A	NCBI36
NG_009029.1:g.6057T>A
NG_028966.1:g.510T>A
NG_009029.2:g.6106T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+127T>A	ENSP00000509954.1:n.328+127T>A
ENST00000378842.8:c.366T>A MANE Select	ENSP00000368119.4:p.Ala122=
ENST00000378842.7:c.366T>A	ENSP00000368119.3:p.Ala122=
ENST00000450095.6:c.51-138T>A	ENSP00000401956.2:n.51-138T>A
ENST00000465543.6:n.705T>A
ENST00000472111.5:n.496T>A
ENST00000473506.6:c.317T>A	ENSP00000432839.2:p.Leu106His
ENST00000473529.5:n.502T>A
ENST00000485531.1:n.681T>A
ENST00000487381.5:n.625T>A
ENST00000489643.6:n.283-421T>A
ENST00000554085.5:c.*110T>A	ENSP00000450419.1:n.*110T>A
ENST00000554139.5:n.419T>A
ENST00000554330.5:n.403T>A
ENST00000554550.5:c.253-138T>A	ENSP00000451435.1:n.253-138T>A
ENST00000554638.5:n.712T>A
ENST00000554897.5:c.253-138T>A	ENSP00000450942.1:n.253-138T>A
ENST00000554944.5:n.436T>A
ENST00000555020.5:n.396T>A
ENST00000555086.5:n.370T>A
ENST00000555214.5:n.262-354T>A
ENST00000556157.1:n.490T>A
ENST00000556244.1:c.353T>A
ENST00000556278.1:c.253-421T>A	ENSP00000451792.1:n.253-421T>A
ENST00000556403.5:n.468T>A
ENST00000556494.5:n.487T>A
ENST00000557541.5:n.510T>A
ENST00000557706.5:n.802T>A
NM_000155.3:c.366T>A	NP_000146.2:p.Ala122=
NM_001258332.1:c.51-138T>A	NP_001245261.1:n.51-138T>A
NM_000155.4:c.366T>A MANE Select	NP_000146.2:p.Ala122=
NM_001258332.2:c.51-138T>A	NP_001245261.1:n.51-138T>A