Canonical Allele Identifier: CA373282154

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648403C>G (hg19) ; chr9:g.34648406C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648406C>G , CM000671.2:g.34648406C>G	GRCh38
NC_000009.11:g.34648403C>G , CM000671.1:g.34648403C>G	GRCh37
NC_000009.10:g.34638403C>G	NCBI36
NG_009029.1:g.6769C>G
NG_028966.1:g.1222C>G
NG_009029.2:g.6818C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*225C>G	ENSP00000509954.1:n.*225C>G
ENST00000378842.8:c.637C>G MANE Select	ENSP00000368119.4:p.His213Asp
ENST00000378842.7:c.637C>G	ENSP00000368119.3:p.His213Asp
ENST00000450095.6:c.310C>G	ENSP00000401956.2:p.His104Asp
ENST00000472111.5:n.893C>G
ENST00000473506.6:c.*225C>G	ENSP00000432839.2:n.*225C>G
ENST00000473529.5:n.796C>G
ENST00000487381.5:n.1022C>G
ENST00000489643.6:n.412C>G
ENST00000554085.5:c.*381C>G	ENSP00000450419.1:n.*381C>G
ENST00000554550.5:c.*257C>G	ENSP00000451435.1:n.*257C>G
ENST00000554638.5:n.1109C>G
ENST00000555020.5:n.793C>G
ENST00000555086.5:n.641C>G
ENST00000555214.5:n.458C>G
ENST00000556244.1:c.624C>G
ENST00000556278.1:c.382C>G	ENSP00000451792.1:p.His128Asp
ENST00000556494.5:n.758C>G
ENST00000557706.5:n.1199C>G
NM_000155.3:c.637C>G	NP_000146.2:p.His213Asp
NM_001258332.1:c.310C>G	NP_001245261.1:p.His104Asp
NM_000155.4:c.637C>G MANE Select	NP_000146.2:p.His213Asp
NM_001258332.2:c.310C>G	NP_001245261.1:p.His104Asp