Canonical Allele Identifier: CA1845640164

Gene: GALT

Linked Data

• dbSNP Id: rs1821180999

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648939G>A , CM000671.2:g.34648939G>A	GRCh38
NC_000009.11:g.34648936G>A , CM000671.1:g.34648936G>A	GRCh37
NC_000009.10:g.34638936G>A	NCBI36
NG_009029.1:g.7302G>A
NG_028966.1:g.1755G>A
NG_009029.2:g.7351G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*408+45G>A	ENSP00000509954.1:n.*408+45G>A
ENST00000378842.8:c.820+45G>A MANE Select	ENSP00000368119.4:n.820+45G>A
ENST00000378842.7:c.820+45G>A	ENSP00000368119.3:n.820+45G>A
ENST00000450095.6:c.493+45G>A	ENSP00000401956.2:n.493+45G>A
ENST00000488412.2:n.18G>A
ENST00000489643.6:n.900+45G>A
ENST00000554085.5:c.*564+45G>A	ENSP00000450419.1:n.*564+45G>A
ENST00000554550.5:c.*440+45G>A	ENSP00000451435.1:n.*440+45G>A
ENST00000554638.5:n.1292+45G>A
ENST00000555020.5:n.1281+45G>A
ENST00000555086.5:n.869G>A
ENST00000555754.1:n.210G>A
ENST00000556278.1:c.432+483G>A	ENSP00000451792.1:n.432+483G>A
ENST00000557706.5:n.1395+32G>A
NM_000155.3:c.820+45G>A	NP_000146.2:n.820+45G>A
NM_001258332.1:c.493+45G>A	NP_001245261.1:n.493+45G>A
NM_000155.4:c.820+45G>A MANE Select	NP_000146.2:n.820+45G>A
NM_001258332.2:c.493+45G>A	NP_001245261.1:n.493+45G>A