Canonical Allele Identifier: CA373282000

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648372G>T (hg19) ; chr9:g.34648375G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648375G>T , CM000671.2:g.34648375G>T	GRCh38
NC_000009.11:g.34648372G>T , CM000671.1:g.34648372G>T	GRCh37
NC_000009.10:g.34638372G>T	NCBI36
NG_009029.1:g.6738G>T
NG_028966.1:g.1191G>T
NG_009029.2:g.6787G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*194G>T	ENSP00000509954.1:n.*194G>T
ENST00000378842.8:c.606G>T MANE Select	ENSP00000368119.4:p.Glu202Asp
ENST00000378842.7:c.606G>T	ENSP00000368119.3:p.Glu202Asp
ENST00000450095.6:c.279G>T	ENSP00000401956.2:p.Glu93Asp
ENST00000472111.5:n.862G>T
ENST00000473506.6:c.*194G>T	ENSP00000432839.2:n.*194G>T
ENST00000473529.5:n.765G>T
ENST00000485531.1:n.1200G>T
ENST00000487381.5:n.991G>T
ENST00000489643.6:n.381G>T
ENST00000554085.5:c.*350G>T	ENSP00000450419.1:n.*350G>T
ENST00000554139.5:n.852G>T
ENST00000554550.5:c.*226G>T	ENSP00000451435.1:n.*226G>T
ENST00000554638.5:n.1078G>T
ENST00000554897.5:c.*293G>T	ENSP00000450942.1:n.*293G>T
ENST00000554944.5:n.955G>T
ENST00000555020.5:n.762G>T
ENST00000555086.5:n.610G>T
ENST00000555214.5:n.427G>T
ENST00000556244.1:c.593G>T
ENST00000556278.1:c.351G>T	ENSP00000451792.1:p.Glu117Asp
ENST00000556494.5:n.727G>T
ENST00000557706.5:n.1168G>T
NM_000155.3:c.606G>T	NP_000146.2:p.Glu202Asp
NM_001258332.1:c.279G>T	NP_001245261.1:p.Glu93Asp
NM_000155.4:c.606G>T MANE Select	NP_000146.2:p.Glu202Asp
NM_001258332.2:c.279G>T	NP_001245261.1:p.Glu93Asp