Canonical Allele Identifier: CA5036227

Gene: GALT

Linked Data

• dbSNP Id: rs763110714
• ExAC: 9:34648973 G / A
• gnomAD v2: 9-34648973-G-A
• gnomAD v3: 9-34648976-G-A
• gnomAD v4: 9-34648976-G-A
• MyVariant Identifiers: chr9:g.34648973G>A (hg19) ; chr9:g.34648976G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648976G>A , CM000671.2:g.34648976G>A	GRCh38
NC_000009.11:g.34648973G>A , CM000671.1:g.34648973G>A	GRCh37
NC_000009.10:g.34638973G>A	NCBI36
NG_009029.1:g.7339G>A
NG_028966.1:g.1792G>A
NG_009029.2:g.7388G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*409-22G>A	ENSP00000509954.1:n.*409-22G>A
ENST00000378842.8:c.821-22G>A MANE Select	ENSP00000368119.4:n.821-22G>A
ENST00000378842.7:c.821-22G>A	ENSP00000368119.3:n.821-22G>A
ENST00000450095.6:c.494-22G>A	ENSP00000401956.2:n.494-22G>A
ENST00000488412.2:n.55G>A
ENST00000489643.6:n.901-22G>A
ENST00000554085.5:c.*565-22G>A	ENSP00000450419.1:n.*565-22G>A
ENST00000554550.5:c.*441-22G>A	ENSP00000451435.1:n.*441-22G>A
ENST00000554638.5:n.1293-22G>A
ENST00000555020.5:n.1282-22G>A
ENST00000555086.5:n.906G>A
ENST00000555754.1:n.247G>A
ENST00000556278.1:c.432+520G>A	ENSP00000451792.1:n.432+520G>A
ENST00000557706.5:n.1396-22G>A
NM_000155.3:c.821-22G>A	NP_000146.2:n.821-22G>A
NM_001258332.1:c.494-22G>A	NP_001245261.1:n.494-22G>A
NM_000155.4:c.821-22G>A MANE Select	NP_000146.2:n.821-22G>A
NM_001258332.2:c.494-22G>A	NP_001245261.1:n.494-22G>A