Canonical Allele Identifier: CA464404519

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649537T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649540T>G , CM000671.2:g.34649540T>G	GRCh38
NC_000009.11:g.34649537T>G , CM000671.1:g.34649537T>G	GRCh37
NC_000009.10:g.34639537T>G	NCBI36
NG_009029.1:g.7903T>G
NG_028966.1:g.2356T>G
NG_009029.2:g.7952T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*623T>G	ENSP00000509954.1:n.*623T>G
ENST00000378842.8:c.1035T>G MANE Select	ENSP00000368119.4:p.Ala345=
ENST00000378842.7:c.1035T>G	ENSP00000368119.3:p.Ala345=
ENST00000450095.6:c.708T>G	ENSP00000401956.2:p.Ala236=
ENST00000488412.2:n.619T>G
ENST00000489643.6:n.1443T>G
ENST00000554550.5:c.*655T>G	ENSP00000451435.1:n.*655T>G
ENST00000554638.5:n.1507T>G
ENST00000555020.5:n.1824T>G
ENST00000555754.1:n.483T>G
ENST00000556278.1:c.432+1084T>G	ENSP00000451792.1:n.432+1084T>G
ENST00000557706.5:n.1610T>G
NM_000155.3:c.1035T>G	NP_000146.2:p.Ala345=
NM_001258332.1:c.708T>G	NP_001245261.1:p.Ala236=
NM_000155.4:c.1035T>G MANE Select	NP_000146.2:p.Ala345=
NM_001258332.2:c.708T>G	NP_001245261.1:p.Ala236=