Canonical Allele Identifier: CA373283656

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648806C>G (hg19) ; chr9:g.34648809C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648809C>G , CM000671.2:g.34648809C>G	GRCh38
NC_000009.11:g.34648806C>G , CM000671.1:g.34648806C>G	GRCh37
NC_000009.10:g.34638806C>G	NCBI36
NG_009029.1:g.7172C>G
NG_028966.1:g.1625C>G
NG_009029.2:g.7221C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*323C>G	ENSP00000509954.1:n.*323C>G
ENST00000378842.8:c.735C>G MANE Select	ENSP00000368119.4:p.Phe245Leu
ENST00000378842.7:c.735C>G	ENSP00000368119.3:p.Phe245Leu
ENST00000450095.6:c.408C>G	ENSP00000401956.2:p.Phe136Leu
ENST00000473506.6:c.*323C>G	ENSP00000432839.2:n.*323C>G
ENST00000473529.5:n.894C>G
ENST00000487381.5:n.1425C>G
ENST00000489643.6:n.815C>G
ENST00000554085.5:c.*479C>G	ENSP00000450419.1:n.*479C>G
ENST00000554550.5:c.*355C>G	ENSP00000451435.1:n.*355C>G
ENST00000554638.5:n.1207C>G
ENST00000555020.5:n.1196C>G
ENST00000555086.5:n.739C>G
ENST00000555754.1:n.80C>G
ENST00000556244.1:c.722C>G
ENST00000556278.1:c.432+353C>G	ENSP00000451792.1:n.432+353C>G
ENST00000557706.5:n.1297C>G
NM_000155.3:c.735C>G	NP_000146.2:p.Phe245Leu
NM_001258332.1:c.408C>G	NP_001245261.1:p.Phe136Leu
NM_000155.4:c.735C>G MANE Select	NP_000146.2:p.Phe245Leu
NM_001258332.2:c.408C>G	NP_001245261.1:p.Phe136Leu