Canonical Allele Identifier: CA373278533

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647109C>G (hg19) ; chr9:g.34647112C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647112C>G , CM000671.2:g.34647112C>G	GRCh38
NC_000009.11:g.34647109C>G , CM000671.1:g.34647109C>G	GRCh37
NC_000009.10:g.34637109C>G	NCBI36
NG_009029.1:g.5475C>G
NG_009029.2:g.5524C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.106C>G	ENSP00000509954.1:p.Pro36Ala
ENST00000378842.8:c.106C>G MANE Select	ENSP00000368119.4:p.Pro36Ala
ENST00000378842.7:c.106C>G	ENSP00000368119.3:p.Pro36Ala
ENST00000450095.6:c.-97C>G	ENSP00000401956.2:n.-97C>G
ENST00000465543.6:n.445C>G
ENST00000468099.2:n.155-9C>G
ENST00000472111.5:n.147C>G
ENST00000473506.6:c.106C>G	ENSP00000432839.2:p.Pro36Ala
ENST00000473529.5:n.153C>G
ENST00000485531.1:n.99C>G
ENST00000487381.5:n.132C>G
ENST00000489643.6:n.136C>G
ENST00000554085.5:c.106C>G	ENSP00000450419.1:p.Pro36Ala
ENST00000554139.5:n.159C>G
ENST00000554330.5:n.103C>G
ENST00000554550.5:c.106C>G	ENSP00000451435.1:p.Pro36Ala
ENST00000554638.5:n.130C>G
ENST00000554897.5:c.106C>G	ENSP00000450942.1:p.Pro36Ala
ENST00000554944.5:n.136C>G
ENST00000555020.5:n.136C>G
ENST00000555086.5:n.110C>G
ENST00000555214.5:n.115C>G
ENST00000556157.1:n.213C>G
ENST00000556278.1:c.106C>G	ENSP00000451792.1:p.Pro36Ala
ENST00000556403.5:n.119C>G
ENST00000556494.5:n.138C>G
ENST00000557541.5:n.299C>G
ENST00000557706.5:n.220C>G
ENST00000605275.1:n.644C>G
NM_000155.3:c.106C>G	NP_000146.2:p.Pro36Ala
NM_001258332.1:c.-97C>G	NP_001245261.1:n.-97C>G
NM_000155.4:c.106C>G MANE Select	NP_000146.2:p.Pro36Ala
NM_001258332.2:c.-97C>G	NP_001245261.1:n.-97C>G