Canonical Allele Identifier: CA464402328

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648435C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648438C>G , CM000671.2:g.34648438C>G	GRCh38
NC_000009.11:g.34648435C>G , CM000671.1:g.34648435C>G	GRCh37
NC_000009.10:g.34638435C>G	NCBI36
NG_009029.1:g.6801C>G
NG_028966.1:g.1254C>G
NG_009029.2:g.6850C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*257C>G	ENSP00000509954.1:n.*257C>G
ENST00000378842.8:c.669C>G MANE Select	ENSP00000368119.4:p.Arg223=
ENST00000378842.7:c.669C>G	ENSP00000368119.3:p.Arg223=
ENST00000450095.6:c.342C>G	ENSP00000401956.2:p.Arg114=
ENST00000472111.5:n.925C>G
ENST00000473506.6:c.*257C>G	ENSP00000432839.2:n.*257C>G
ENST00000473529.5:n.828C>G
ENST00000487381.5:n.1054C>G
ENST00000489643.6:n.444C>G
ENST00000554085.5:c.*413C>G	ENSP00000450419.1:n.*413C>G
ENST00000554550.5:c.*289C>G	ENSP00000451435.1:n.*289C>G
ENST00000554638.5:n.1141C>G
ENST00000555020.5:n.825C>G
ENST00000555086.5:n.673C>G
ENST00000555214.5:n.490C>G
ENST00000555754.1:n.14C>G
ENST00000556244.1:c.656C>G
ENST00000556278.1:c.414C>G	ENSP00000451792.1:p.Arg138=
ENST00000556494.5:n.790C>G
ENST00000557706.5:n.1231C>G
NM_000155.3:c.669C>G	NP_000146.2:p.Arg223=
NM_001258332.1:c.342C>G	NP_001245261.1:p.Arg114=
NM_000155.4:c.669C>G MANE Select	NP_000146.2:p.Arg223=
NM_001258332.2:c.342C>G	NP_001245261.1:p.Arg114=