Canonical Allele Identifier: CA464403320

Gene: GALT

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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