Canonical Allele Identifier: CA464401897

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648159C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648162C>A , CM000671.2:g.34648162C>A	GRCh38
NC_000009.11:g.34648159C>A , CM000671.1:g.34648159C>A	GRCh37
NC_000009.10:g.34638159C>A	NCBI36
NG_009029.1:g.6525C>A
NG_028966.1:g.978C>A
NG_009029.2:g.6574C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*143C>A	ENSP00000509954.1:n.*143C>A
ENST00000378842.8:c.555C>A MANE Select	ENSP00000368119.4:p.Pro185=
ENST00000378842.7:c.555C>A	ENSP00000368119.3:p.Pro185=
ENST00000450095.6:c.228C>A	ENSP00000401956.2:p.Pro76=
ENST00000465543.6:n.894C>A
ENST00000472111.5:n.811C>A
ENST00000473506.6:c.*143C>A	ENSP00000432839.2:n.*143C>A
ENST00000473529.5:n.714C>A
ENST00000485531.1:n.1149C>A
ENST00000487381.5:n.940C>A
ENST00000489643.6:n.330C>A
ENST00000554085.5:c.*299C>A	ENSP00000450419.1:n.*299C>A
ENST00000554139.5:n.801C>A
ENST00000554550.5:c.*175C>A	ENSP00000451435.1:n.*175C>A
ENST00000554638.5:n.1027C>A
ENST00000554897.5:c.*242C>A	ENSP00000450942.1:n.*242C>A
ENST00000554944.5:n.904C>A
ENST00000555020.5:n.711C>A
ENST00000555086.5:n.559C>A
ENST00000555214.5:n.376C>A
ENST00000556244.1:c.542C>A
ENST00000556278.1:c.300C>A	ENSP00000451792.1:p.Pro100=
ENST00000556494.5:n.676C>A
ENST00000557706.5:n.1117C>A
NM_000155.3:c.555C>A	NP_000146.2:p.Pro185=
NM_001258332.1:c.228C>A	NP_001245261.1:p.Pro76=
NM_000155.4:c.555C>A MANE Select	NP_000146.2:p.Pro185=
NM_001258332.2:c.228C>A	NP_001245261.1:p.Pro76=