Canonical Allele Identifier: CA373280381

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647678A>T (hg19) ; chr9:g.34647681A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647681A>T , CM000671.2:g.34647681A>T	GRCh38
NC_000009.11:g.34647678A>T , CM000671.1:g.34647678A>T	GRCh37
NC_000009.10:g.34637678A>T	NCBI36
NG_009029.1:g.6044A>T
NG_028966.1:g.497A>T
NG_009029.2:g.6093A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+114A>T	ENSP00000509954.1:n.328+114A>T
ENST00000378842.8:c.353A>T MANE Select	ENSP00000368119.4:p.Gln118Leu
ENST00000378842.7:c.353A>T	ENSP00000368119.3:p.Gln118Leu
ENST00000450095.6:c.51-151A>T	ENSP00000401956.2:n.51-151A>T
ENST00000465543.6:n.692A>T
ENST00000472111.5:n.483A>T
ENST00000473506.6:c.304A>T	ENSP00000432839.2:p.Lys102Ter
ENST00000473529.5:n.489A>T
ENST00000485531.1:n.668A>T
ENST00000487381.5:n.612A>T
ENST00000489643.6:n.282+423A>T
ENST00000554085.5:c.*97A>T	ENSP00000450419.1:n.*97A>T
ENST00000554139.5:n.406A>T
ENST00000554330.5:n.390A>T
ENST00000554550.5:c.253-151A>T	ENSP00000451435.1:n.253-151A>T
ENST00000554638.5:n.699A>T
ENST00000554897.5:c.253-151A>T	ENSP00000450942.1:n.253-151A>T
ENST00000554944.5:n.423A>T
ENST00000555020.5:n.383A>T
ENST00000555086.5:n.357A>T
ENST00000555214.5:n.262-367A>T
ENST00000556157.1:n.477A>T
ENST00000556244.1:c.340A>T
ENST00000556278.1:c.252+423A>T	ENSP00000451792.1:n.252+423A>T
ENST00000556403.5:n.455A>T
ENST00000556494.5:n.474A>T
ENST00000557541.5:n.497A>T
ENST00000557706.5:n.789A>T
NM_000155.3:c.353A>T	NP_000146.2:p.Gln118Leu
NM_001258332.1:c.51-151A>T	NP_001245261.1:n.51-151A>T
NM_000155.4:c.353A>T MANE Select	NP_000146.2:p.Gln118Leu
NM_001258332.2:c.51-151A>T	NP_001245261.1:n.51-151A>T