Canonical Allele Identifier: CA464404012

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649071C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649074C>T , CM000671.2:g.34649074C>T	GRCh38
NC_000009.11:g.34649071C>T , CM000671.1:g.34649071C>T	GRCh37
NC_000009.10:g.34639071C>T	NCBI36
NG_009029.1:g.7437C>T
NG_028966.1:g.1890C>T
NG_009029.2:g.7486C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*485C>T	ENSP00000509954.1:n.*485C>T
ENST00000378842.8:c.897C>T MANE Select	ENSP00000368119.4:p.Gly299=
ENST00000378842.7:c.897C>T	ENSP00000368119.3:p.Gly299=
ENST00000450095.6:c.570C>T	ENSP00000401956.2:p.Gly190=
ENST00000488412.2:n.153C>T
ENST00000489643.6:n.977C>T
ENST00000554550.5:c.*517C>T	ENSP00000451435.1:n.*517C>T
ENST00000554638.5:n.1369C>T
ENST00000555020.5:n.1358C>T
ENST00000555086.5:n.1004C>T
ENST00000555754.1:n.345C>T
ENST00000556278.1:c.432+618C>T	ENSP00000451792.1:n.432+618C>T
ENST00000557706.5:n.1472C>T
NM_000155.3:c.897C>T	NP_000146.2:p.Gly299=
NM_001258332.1:c.570C>T	NP_001245261.1:p.Gly190=
NM_000155.4:c.897C>T MANE Select	NP_000146.2:p.Gly299=
NM_001258332.2:c.570C>T	NP_001245261.1:p.Gly190=