Canonical Allele Identifier: CA464595788

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647655A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647658A>G , CM000671.2:g.34647658A>G	GRCh38
NC_000009.11:g.34647655A>G , CM000671.1:g.34647655A>G	GRCh37
NC_000009.10:g.34637655A>G	NCBI36
NG_009029.1:g.6021A>G
NG_028966.1:g.474A>G
NG_009029.2:g.6070A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+91A>G	ENSP00000509954.1:n.328+91A>G
ENST00000378842.8:c.330A>G MANE Select	ENSP00000368119.4:p.Gly110=
ENST00000378842.7:c.330A>G	ENSP00000368119.3:p.Gly110=
ENST00000450095.6:c.51-174A>G	ENSP00000401956.2:n.51-174A>G
ENST00000465543.6:n.669A>G
ENST00000472111.5:n.460A>G
ENST00000473506.6:c.281A>G	ENSP00000432839.2:p.Asp94Gly
ENST00000473529.5:n.466A>G
ENST00000485531.1:n.645A>G
ENST00000487381.5:n.589A>G
ENST00000489643.6:n.282+400A>G
ENST00000554085.5:c.*74A>G	ENSP00000450419.1:n.*74A>G
ENST00000554139.5:n.383A>G
ENST00000554330.5:n.367A>G
ENST00000554550.5:c.253-174A>G	ENSP00000451435.1:n.253-174A>G
ENST00000554638.5:n.676A>G
ENST00000554897.5:c.253-174A>G	ENSP00000450942.1:n.253-174A>G
ENST00000554944.5:n.400A>G
ENST00000555020.5:n.360A>G
ENST00000555086.5:n.334A>G
ENST00000555214.5:n.262-390A>G
ENST00000556157.1:n.454A>G
ENST00000556244.1:c.317A>G
ENST00000556278.1:c.252+400A>G	ENSP00000451792.1:n.252+400A>G
ENST00000556403.5:n.432A>G
ENST00000556494.5:n.451A>G
ENST00000557541.5:n.474A>G
ENST00000557706.5:n.766A>G
NM_000155.3:c.330A>G	NP_000146.2:p.Gly110=
NM_001258332.1:c.51-174A>G	NP_001245261.1:n.51-174A>G
NM_000155.4:c.330A>G MANE Select	NP_000146.2:p.Gly110=
NM_001258332.2:c.51-174A>G	NP_001245261.1:n.51-174A>G