Canonical Allele Identifier: CA464595797

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647658C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647661C>G , CM000671.2:g.34647661C>G	GRCh38
NC_000009.11:g.34647658C>G , CM000671.1:g.34647658C>G	GRCh37
NC_000009.10:g.34637658C>G	NCBI36
NG_009029.1:g.6024C>G
NG_028966.1:g.477C>G
NG_009029.2:g.6073C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.328+94C>G	ENSP00000509954.1:n.328+94C>G
ENST00000378842.8:c.333C>G MANE Select	ENSP00000368119.4:p.Pro111=
ENST00000378842.7:c.333C>G	ENSP00000368119.3:p.Pro111=
ENST00000450095.6:c.51-171C>G	ENSP00000401956.2:n.51-171C>G
ENST00000465543.6:n.672C>G
ENST00000472111.5:n.463C>G
ENST00000473506.6:c.284C>G	ENSP00000432839.2:p.Pro95Arg
ENST00000473529.5:n.469C>G
ENST00000485531.1:n.648C>G
ENST00000487381.5:n.592C>G
ENST00000489643.6:n.282+403C>G
ENST00000554085.5:c.*77C>G	ENSP00000450419.1:n.*77C>G
ENST00000554139.5:n.386C>G
ENST00000554330.5:n.370C>G
ENST00000554550.5:c.253-171C>G	ENSP00000451435.1:n.253-171C>G
ENST00000554638.5:n.679C>G
ENST00000554897.5:c.253-171C>G	ENSP00000450942.1:n.253-171C>G
ENST00000554944.5:n.403C>G
ENST00000555020.5:n.363C>G
ENST00000555086.5:n.337C>G
ENST00000555214.5:n.262-387C>G
ENST00000556157.1:n.457C>G
ENST00000556244.1:c.320C>G
ENST00000556278.1:c.252+403C>G	ENSP00000451792.1:n.252+403C>G
ENST00000556403.5:n.435C>G
ENST00000556494.5:n.454C>G
ENST00000557541.5:n.477C>G
ENST00000557706.5:n.769C>G
NM_000155.3:c.333C>G	NP_000146.2:p.Pro111=
NM_001258332.1:c.51-171C>G	NP_001245261.1:n.51-171C>G
NM_000155.4:c.333C>G MANE Select	NP_000146.2:p.Pro111=
NM_001258332.2:c.51-171C>G	NP_001245261.1:n.51-171C>G