Canonical Allele Identifier: CA373283886

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648841C>G (hg19) ; chr9:g.34648844C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648844C>G , CM000671.2:g.34648844C>G	GRCh38
NC_000009.11:g.34648841C>G , CM000671.1:g.34648841C>G	GRCh37
NC_000009.10:g.34638841C>G	NCBI36
NG_009029.1:g.7207C>G
NG_028966.1:g.1660C>G
NG_009029.2:g.7256C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*358C>G	ENSP00000509954.1:n.*358C>G
ENST00000378842.8:c.770C>G MANE Select	ENSP00000368119.4:p.Pro257Arg
ENST00000378842.7:c.770C>G	ENSP00000368119.3:p.Pro257Arg
ENST00000450095.6:c.443C>G	ENSP00000401956.2:p.Pro148Arg
ENST00000473506.6:c.*358C>G	ENSP00000432839.2:n.*358C>G
ENST00000489643.6:n.850C>G
ENST00000554085.5:c.*514C>G	ENSP00000450419.1:n.*514C>G
ENST00000554550.5:c.*390C>G	ENSP00000451435.1:n.*390C>G
ENST00000554638.5:n.1242C>G
ENST00000555020.5:n.1231C>G
ENST00000555086.5:n.774C>G
ENST00000555754.1:n.115C>G
ENST00000556244.1:c.757C>G
ENST00000556278.1:c.432+388C>G	ENSP00000451792.1:n.432+388C>G
ENST00000557706.5:n.1332C>G
NM_000155.3:c.770C>G	NP_000146.2:p.Pro257Arg
NM_001258332.1:c.443C>G	NP_001245261.1:p.Pro148Arg
NM_000155.4:c.770C>G MANE Select	NP_000146.2:p.Pro257Arg
NM_001258332.2:c.443C>G	NP_001245261.1:p.Pro148Arg