Canonical Allele Identifier: CA373278603

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647144C>G (hg19) ; chr9:g.34647147C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647147C>G , CM000671.2:g.34647147C>G	GRCh38
NC_000009.11:g.34647144C>G , CM000671.1:g.34647144C>G	GRCh37
NC_000009.10:g.34637144C>G	NCBI36
NG_009029.1:g.5510C>G
NG_009029.2:g.5559C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.141C>G	ENSP00000509954.1:p.His47Gln
ENST00000378842.8:c.141C>G MANE Select	ENSP00000368119.4:p.His47Gln
ENST00000378842.7:c.141C>G	ENSP00000368119.3:p.His47Gln
ENST00000450095.6:c.-62C>G	ENSP00000401956.2:n.-62C>G
ENST00000465543.6:n.480C>G
ENST00000468099.2:n.181C>G
ENST00000472111.5:n.182C>G
ENST00000473506.6:c.141C>G	ENSP00000432839.2:p.His47Gln
ENST00000473529.5:n.188C>G
ENST00000485531.1:n.134C>G
ENST00000487381.5:n.167C>G
ENST00000489643.6:n.171C>G
ENST00000554085.5:c.141C>G	ENSP00000450419.1:p.His47Gln
ENST00000554139.5:n.194C>G
ENST00000554330.5:n.138C>G
ENST00000554550.5:c.141C>G	ENSP00000451435.1:p.His47Gln
ENST00000554638.5:n.165C>G
ENST00000554897.5:c.141C>G	ENSP00000450942.1:p.His47Gln
ENST00000554944.5:n.171C>G
ENST00000555020.5:n.171C>G
ENST00000555086.5:n.145C>G
ENST00000555214.5:n.150C>G
ENST00000556157.1:n.248C>G
ENST00000556244.1:c.25C>G
ENST00000556278.1:c.141C>G	ENSP00000451792.1:p.His47Gln
ENST00000556403.5:n.154C>G
ENST00000556494.5:n.173C>G
ENST00000557541.5:n.334C>G
ENST00000557706.5:n.255C>G
NM_000155.3:c.141C>G	NP_000146.2:p.His47Gln
NM_001258332.1:c.-62C>G	NP_001245261.1:n.-62C>G
NM_000155.4:c.141C>G MANE Select	NP_000146.2:p.His47Gln
NM_001258332.2:c.-62C>G	NP_001245261.1:n.-62C>G