Canonical Allele Identifier: CA5035981

Gene: GALT

Linked Data

• dbSNP Id: rs761685630
• ExAC: 9:34646701 C / A
• gnomAD v2: 9-34646701-C-A
• gnomAD v4: 9-34646704-C-A
• MyVariant Identifiers: chr9:g.34646701C>A (hg19) ; chr9:g.34646704C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646704C>A , CM000671.2:g.34646704C>A	GRCh38
NC_000009.11:g.34646701C>A , CM000671.1:g.34646701C>A	GRCh37
NC_000009.10:g.34636701C>A	NCBI36
NG_009029.1:g.5067C>A
NG_009029.2:g.5116C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.-1C>A	ENSP00000509954.1:n.-1C>A
ENST00000378842.8:c.-1C>A MANE Select	ENSP00000368119.4:n.-1C>A
ENST00000378842.7:c.-1C>A	ENSP00000368119.3:n.-1C>A
ENST00000450095.6:c.-203C>A	ENSP00000401956.2:n.-203C>A
ENST00000465543.6:n.37C>A
ENST00000468099.2:n.72C>A
ENST00000472111.5:n.41C>A
ENST00000473506.6:c.-1C>A	ENSP00000432839.2:n.-1C>A
ENST00000473529.5:n.47C>A
ENST00000487381.5:n.26C>A
ENST00000489643.6:n.30C>A
ENST00000554085.5:c.-1C>A	ENSP00000450419.1:n.-1C>A
ENST00000554139.5:n.53C>A
ENST00000554550.5:c.-1C>A	ENSP00000451435.1:n.-1C>A
ENST00000554638.5:n.24C>A
ENST00000554897.5:c.-1C>A	ENSP00000450942.1:n.-1C>A
ENST00000554944.5:n.30C>A
ENST00000555020.5:n.30C>A
ENST00000555214.5:n.9C>A
ENST00000556278.1:c.-1C>A	ENSP00000451792.1:n.-1C>A
ENST00000557541.5:n.60C>A
ENST00000605275.1:n.236C>A
NM_000155.3:c.-1C>A	NP_000146.2:n.-1C>A
NM_001258332.1:c.-203C>A	NP_001245261.1:n.-203C>A
NM_000155.4:c.-1C>A MANE Select	NP_000146.2:n.-1C>A
NM_001258332.2:c.-203C>A	NP_001245261.1:n.-203C>A