Canonical Allele Identifier: CA464404488

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649531T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649534T>A , CM000671.2:g.34649534T>A	GRCh38
NC_000009.11:g.34649531T>A , CM000671.1:g.34649531T>A	GRCh37
NC_000009.10:g.34639531T>A	NCBI36
NG_009029.1:g.7897T>A
NG_028966.1:g.2350T>A
NG_009029.2:g.7946T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*617T>A	ENSP00000509954.1:n.*617T>A
ENST00000378842.8:c.1029T>A MANE Select	ENSP00000368119.4:p.Ala343=
ENST00000378842.7:c.1029T>A	ENSP00000368119.3:p.Ala343=
ENST00000450095.6:c.702T>A	ENSP00000401956.2:p.Ala234=
ENST00000488412.2:n.613T>A
ENST00000489643.6:n.1437T>A
ENST00000554550.5:c.*649T>A	ENSP00000451435.1:n.*649T>A
ENST00000554638.5:n.1501T>A
ENST00000555020.5:n.1818T>A
ENST00000555754.1:n.477T>A
ENST00000556278.1:c.432+1078T>A	ENSP00000451792.1:n.432+1078T>A
ENST00000557706.5:n.1604T>A
NM_000155.3:c.1029T>A	NP_000146.2:p.Ala343=
NM_001258332.1:c.702T>A	NP_001245261.1:p.Ala234=
NM_000155.4:c.1029T>A MANE Select	NP_000146.2:p.Ala343=
NM_001258332.2:c.702T>A	NP_001245261.1:p.Ala234=