Canonical Allele Identifier: CA373284889

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649460G>T (hg19) ; chr9:g.34649463G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649463G>T , CM000671.2:g.34649463G>T	GRCh38
NC_000009.11:g.34649460G>T , CM000671.1:g.34649460G>T	GRCh37
NC_000009.10:g.34639460G>T	NCBI36
NG_009029.1:g.7826G>T
NG_028966.1:g.2279G>T
NG_009029.2:g.7875G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*546G>T	ENSP00000509954.1:n.*546G>T
ENST00000378842.8:c.958G>T MANE Select	ENSP00000368119.4:p.Ala320Ser
ENST00000378842.7:c.958G>T	ENSP00000368119.3:p.Ala320Ser
ENST00000450095.6:c.631G>T	ENSP00000401956.2:p.Ala211Ser
ENST00000488412.2:n.542G>T
ENST00000489643.6:n.1366G>T
ENST00000554550.5:c.*578G>T	ENSP00000451435.1:n.*578G>T
ENST00000554638.5:n.1430G>T
ENST00000555020.5:n.1747G>T
ENST00000555754.1:n.406G>T
ENST00000556278.1:c.432+1007G>T	ENSP00000451792.1:n.432+1007G>T
ENST00000557706.5:n.1533G>T
NM_000155.3:c.958G>T	NP_000146.2:p.Ala320Ser
NM_001258332.1:c.631G>T	NP_001245261.1:p.Ala211Ser
NM_000155.4:c.958G>T MANE Select	NP_000146.2:p.Ala320Ser
NM_001258332.2:c.631G>T	NP_001245261.1:p.Ala211Ser