Canonical Allele Identifier: CA373283778

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648819C>G (hg19) ; chr9:g.34648822C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648822C>G , CM000671.2:g.34648822C>G	GRCh38
NC_000009.11:g.34648819C>G , CM000671.1:g.34648819C>G	GRCh37
NC_000009.10:g.34638819C>G	NCBI36
NG_009029.1:g.7185C>G
NG_028966.1:g.1638C>G
NG_009029.2:g.7234C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*336C>G	ENSP00000509954.1:n.*336C>G
ENST00000378842.8:c.748C>G MANE Select	ENSP00000368119.4:p.Pro250Ala
ENST00000378842.7:c.748C>G	ENSP00000368119.3:p.Pro250Ala
ENST00000450095.6:c.421C>G	ENSP00000401956.2:p.Pro141Ala
ENST00000473506.6:c.*336C>G	ENSP00000432839.2:n.*336C>G
ENST00000473529.5:n.907C>G
ENST00000487381.5:n.1438C>G
ENST00000489643.6:n.828C>G
ENST00000554085.5:c.*492C>G	ENSP00000450419.1:n.*492C>G
ENST00000554550.5:c.*368C>G	ENSP00000451435.1:n.*368C>G
ENST00000554638.5:n.1220C>G
ENST00000555020.5:n.1209C>G
ENST00000555086.5:n.752C>G
ENST00000555754.1:n.93C>G
ENST00000556244.1:c.735C>G
ENST00000556278.1:c.432+366C>G	ENSP00000451792.1:n.432+366C>G
ENST00000557706.5:n.1310C>G
NM_000155.3:c.748C>G	NP_000146.2:p.Pro250Ala
NM_001258332.1:c.421C>G	NP_001245261.1:p.Pro141Ala
NM_000155.4:c.748C>G MANE Select	NP_000146.2:p.Pro250Ala
NM_001258332.2:c.421C>G	NP_001245261.1:p.Pro141Ala