Canonical Allele Identifier: CA373278591

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647139G>A (hg19) ; chr9:g.34647142G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647142G>A , CM000671.2:g.34647142G>A	GRCh38
NC_000009.11:g.34647139G>A , CM000671.1:g.34647139G>A	GRCh37
NC_000009.10:g.34637139G>A	NCBI36
NG_009029.1:g.5505G>A
NG_009029.2:g.5554G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.136G>A	ENSP00000509954.1:p.Ala46Thr
ENST00000378842.8:c.136G>A MANE Select	ENSP00000368119.4:p.Ala46Thr
ENST00000378842.7:c.136G>A	ENSP00000368119.3:p.Ala46Thr
ENST00000450095.6:c.-67G>A	ENSP00000401956.2:n.-67G>A
ENST00000465543.6:n.475G>A
ENST00000468099.2:n.176G>A
ENST00000472111.5:n.177G>A
ENST00000473506.6:c.136G>A	ENSP00000432839.2:p.Ala46Thr
ENST00000473529.5:n.183G>A
ENST00000485531.1:n.129G>A
ENST00000487381.5:n.162G>A
ENST00000489643.6:n.166G>A
ENST00000554085.5:c.136G>A	ENSP00000450419.1:p.Ala46Thr
ENST00000554139.5:n.189G>A
ENST00000554330.5:n.133G>A
ENST00000554550.5:c.136G>A	ENSP00000451435.1:p.Ala46Thr
ENST00000554638.5:n.160G>A
ENST00000554897.5:c.136G>A	ENSP00000450942.1:p.Ala46Thr
ENST00000554944.5:n.166G>A
ENST00000555020.5:n.166G>A
ENST00000555086.5:n.140G>A
ENST00000555214.5:n.145G>A
ENST00000556157.1:n.243G>A
ENST00000556244.1:c.20G>A
ENST00000556278.1:c.136G>A	ENSP00000451792.1:p.Ala46Thr
ENST00000556403.5:n.149G>A
ENST00000556494.5:n.168G>A
ENST00000557541.5:n.329G>A
ENST00000557706.5:n.250G>A
ENST00000605275.1:n.674G>A
NM_000155.3:c.136G>A	NP_000146.2:p.Ala46Thr
NM_001258332.1:c.-67G>A	NP_001245261.1:n.-67G>A
NM_000155.4:c.136G>A MANE Select	NP_000146.2:p.Ala46Thr
NM_001258332.2:c.-67G>A	NP_001245261.1:n.-67G>A