Canonical Allele Identifier: CA5036031

Gene: GALT

Linked Data

• ClinVar Variation Id: 1671309
• ClinVar RCV Id: RCV002196680
• dbSNP Id: rs766778777
• ExAC: 9:34647165 G / A
• gnomAD v2: 9-34647165-G-A
• gnomAD v4: 9-34647168-G-A
• MyVariant Identifiers: chr9:g.34647165G>A (hg19) ; chr9:g.34647168G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647168G>A , CM000671.2:g.34647168G>A	GRCh38
NC_000009.11:g.34647165G>A , CM000671.1:g.34647165G>A	GRCh37
NC_000009.10:g.34637165G>A	NCBI36
NG_009029.1:g.5531G>A
NG_009029.2:g.5580G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.162G>A	ENSP00000509954.1:p.Gln54=
ENST00000378842.8:c.162G>A MANE Select	ENSP00000368119.4:p.Gln54=
ENST00000378842.7:c.162G>A	ENSP00000368119.3:p.Gln54=
ENST00000450095.6:c.-41G>A	ENSP00000401956.2:n.-41G>A
ENST00000465543.6:n.501G>A
ENST00000468099.2:n.202G>A
ENST00000472111.5:n.203G>A
ENST00000473506.6:c.162G>A	ENSP00000432839.2:p.Gln54=
ENST00000473529.5:n.209G>A
ENST00000485531.1:n.155G>A
ENST00000487381.5:n.188G>A
ENST00000489643.6:n.192G>A
ENST00000554085.5:c.162G>A	ENSP00000450419.1:p.Gln54=
ENST00000554139.5:n.215G>A
ENST00000554330.5:n.159G>A
ENST00000554550.5:c.162G>A	ENSP00000451435.1:p.Gln54=
ENST00000554638.5:n.186G>A
ENST00000554897.5:c.162G>A	ENSP00000450942.1:p.Gln54=
ENST00000554944.5:n.192G>A
ENST00000555020.5:n.192G>A
ENST00000555086.5:n.166G>A
ENST00000555214.5:n.171G>A
ENST00000556157.1:n.269G>A
ENST00000556244.1:c.46G>A
ENST00000556278.1:c.162G>A	ENSP00000451792.1:p.Gln54=
ENST00000556403.5:n.175G>A
ENST00000556494.5:n.194G>A
ENST00000557541.5:n.355G>A
ENST00000557706.5:n.276G>A
NM_000155.3:c.162G>A	NP_000146.2:p.Gln54=
NM_001258332.1:c.-41G>A	NP_001245261.1:n.-41G>A
NM_000155.4:c.162G>A MANE Select	NP_000146.2:p.Gln54=
NM_001258332.2:c.-41G>A	NP_001245261.1:n.-41G>A