Canonical Allele Identifier: CA863494262

Gene: GALT

Linked Data

• dbSNP Id: rs1490502692
• MyVariant Identifiers: chr9:g.34647017T>G (hg19) ; chr9:g.34647020T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647020T>G , CM000671.2:g.34647020T>G	GRCh38
NC_000009.11:g.34647017T>G , CM000671.1:g.34647017T>G	GRCh37
NC_000009.10:g.34637017T>G	NCBI36
NG_009029.1:g.5383T>G
NG_009029.2:g.5432T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.83-69T>G	ENSP00000509954.1:n.83-69T>G
ENST00000378842.8:c.83-69T>G MANE Select	ENSP00000368119.4:n.83-69T>G
ENST00000378842.7:c.83-69T>G	ENSP00000368119.3:n.83-69T>G
ENST00000450095.6:c.-120-69T>G	ENSP00000401956.2:n.-120-69T>G
ENST00000465543.6:n.353T>G
ENST00000468099.2:n.155-101T>G
ENST00000472111.5:n.124-69T>G
ENST00000473506.6:c.83-69T>G	ENSP00000432839.2:n.83-69T>G
ENST00000473529.5:n.130-69T>G
ENST00000485531.1:n.76-69T>G
ENST00000487381.5:n.109-69T>G
ENST00000489643.6:n.113-69T>G
ENST00000554085.5:c.83-69T>G	ENSP00000450419.1:n.83-69T>G
ENST00000554139.5:n.136-69T>G
ENST00000554330.5:n.80-69T>G
ENST00000554550.5:c.83-69T>G	ENSP00000451435.1:n.83-69T>G
ENST00000554638.5:n.107-69T>G
ENST00000554897.5:c.83-69T>G	ENSP00000450942.1:n.83-69T>G
ENST00000554944.5:n.113-69T>G
ENST00000555020.5:n.113-69T>G
ENST00000555086.5:n.87-69T>G
ENST00000555214.5:n.92-69T>G
ENST00000556157.1:n.121T>G
ENST00000556278.1:c.83-69T>G	ENSP00000451792.1:n.83-69T>G
ENST00000556403.5:n.96-69T>G
ENST00000556494.5:n.115-69T>G
ENST00000557541.5:n.276-69T>G
ENST00000557706.5:n.128T>G
ENST00000605275.1:n.552T>G
NM_000155.3:c.83-69T>G	NP_000146.2:n.83-69T>G
NM_001258332.1:c.-120-69T>G	NP_001245261.1:n.-120-69T>G
NM_000155.4:c.83-69T>G MANE Select	NP_000146.2:n.83-69T>G
NM_001258332.2:c.-120-69T>G	NP_001245261.1:n.-120-69T>G