Canonical Allele Identifier: CA464403322

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648881T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648884T>G , CM000671.2:g.34648884T>G	GRCh38
NC_000009.11:g.34648881T>G , CM000671.1:g.34648881T>G	GRCh37
NC_000009.10:g.34638881T>G	NCBI36
NG_009029.1:g.7247T>G
NG_028966.1:g.1700T>G
NG_009029.2:g.7296T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*398T>G	ENSP00000509954.1:n.*398T>G
ENST00000378842.8:c.810T>G MANE Select	ENSP00000368119.4:p.Ala270=
ENST00000378842.7:c.810T>G	ENSP00000368119.3:p.Ala270=
ENST00000450095.6:c.483T>G	ENSP00000401956.2:p.Ala161=
ENST00000473506.6:c.*398T>G	ENSP00000432839.2:n.*398T>G
ENST00000489643.6:n.890T>G
ENST00000554085.5:c.*554T>G	ENSP00000450419.1:n.*554T>G
ENST00000554550.5:c.*430T>G	ENSP00000451435.1:n.*430T>G
ENST00000554638.5:n.1282T>G
ENST00000555020.5:n.1271T>G
ENST00000555086.5:n.814T>G
ENST00000555754.1:n.155T>G
ENST00000556244.1:c.797T>G
ENST00000556278.1:c.432+428T>G	ENSP00000451792.1:n.432+428T>G
ENST00000557706.5:n.1372T>G
NM_000155.3:c.810T>G	NP_000146.2:p.Ala270=
NM_001258332.1:c.483T>G	NP_001245261.1:p.Ala161=
NM_000155.4:c.810T>G MANE Select	NP_000146.2:p.Ala270=
NM_001258332.2:c.483T>G	NP_001245261.1:p.Ala161=