Canonical Allele Identifier: CA464401968

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648339C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648342C>G , CM000671.2:g.34648342C>G	GRCh38
NC_000009.11:g.34648339C>G , CM000671.1:g.34648339C>G	GRCh37
NC_000009.10:g.34638339C>G	NCBI36
NG_009029.1:g.6705C>G
NG_028966.1:g.1158C>G
NG_009029.2:g.6754C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*161C>G	ENSP00000509954.1:n.*161C>G
ENST00000378842.8:c.573C>G MANE Select	ENSP00000368119.4:p.Ala191=
ENST00000378842.7:c.573C>G	ENSP00000368119.3:p.Ala191=
ENST00000450095.6:c.246C>G	ENSP00000401956.2:p.Ala82=
ENST00000472111.5:n.829C>G
ENST00000473506.6:c.*161C>G	ENSP00000432839.2:n.*161C>G
ENST00000473529.5:n.732C>G
ENST00000485531.1:n.1167C>G
ENST00000487381.5:n.958C>G
ENST00000489643.6:n.348C>G
ENST00000554085.5:c.*317C>G	ENSP00000450419.1:n.*317C>G
ENST00000554139.5:n.819C>G
ENST00000554550.5:c.*193C>G	ENSP00000451435.1:n.*193C>G
ENST00000554638.5:n.1045C>G
ENST00000554897.5:c.*260C>G	ENSP00000450942.1:n.*260C>G
ENST00000554944.5:n.922C>G
ENST00000555020.5:n.729C>G
ENST00000555086.5:n.577C>G
ENST00000555214.5:n.394C>G
ENST00000556244.1:c.560C>G
ENST00000556278.1:c.318C>G	ENSP00000451792.1:p.Ala106=
ENST00000556494.5:n.694C>G
ENST00000557706.5:n.1135C>G
NM_000155.3:c.573C>G	NP_000146.2:p.Ala191=
NM_001258332.1:c.246C>G	NP_001245261.1:p.Ala82=
NM_000155.4:c.573C>G MANE Select	NP_000146.2:p.Ala191=
NM_001258332.2:c.246C>G	NP_001245261.1:p.Ala82=