Canonical Allele Identifier: CA464403230

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648858C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648861C>A , CM000671.2:g.34648861C>A	GRCh38
NC_000009.11:g.34648858C>A , CM000671.1:g.34648858C>A	GRCh37
NC_000009.10:g.34638858C>A	NCBI36
NG_009029.1:g.7224C>A
NG_028966.1:g.1677C>A
NG_009029.2:g.7273C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*375C>A	ENSP00000509954.1:n.*375C>A
ENST00000378842.8:c.787C>A MANE Select	ENSP00000368119.4:p.Arg263=
ENST00000378842.7:c.787C>A	ENSP00000368119.3:p.Arg263=
ENST00000450095.6:c.460C>A	ENSP00000401956.2:p.Arg154=
ENST00000473506.6:c.*375C>A	ENSP00000432839.2:n.*375C>A
ENST00000489643.6:n.867C>A
ENST00000554085.5:c.*531C>A	ENSP00000450419.1:n.*531C>A
ENST00000554550.5:c.*407C>A	ENSP00000451435.1:n.*407C>A
ENST00000554638.5:n.1259C>A
ENST00000555020.5:n.1248C>A
ENST00000555086.5:n.791C>A
ENST00000555754.1:n.132C>A
ENST00000556244.1:c.774C>A
ENST00000556278.1:c.432+405C>A	ENSP00000451792.1:n.432+405C>A
ENST00000557706.5:n.1349C>A
NM_000155.3:c.787C>A	NP_000146.2:p.Arg263=
NM_001258332.1:c.460C>A	NP_001245261.1:p.Arg154=
NM_000155.4:c.787C>A MANE Select	NP_000146.2:p.Arg263=
NM_001258332.2:c.460C>A	NP_001245261.1:p.Arg154=