Canonical Allele Identifier: CA1845635092

Gene: GALT

Linked Data

• dbSNP Id: rs1587236781
• gnomAD v4: 9-34646934-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646934C>A , CM000671.2:g.34646934C>A	GRCh38
NC_000009.11:g.34646931C>A , CM000671.1:g.34646931C>A	GRCh37
NC_000009.10:g.34636931C>A	NCBI36
NG_009029.1:g.5297C>A
NG_009029.2:g.5346C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.82+148C>A	ENSP00000509954.1:n.82+148C>A
ENST00000378842.8:c.82+148C>A MANE Select	ENSP00000368119.4:n.82+148C>A
ENST00000378842.7:c.82+148C>A	ENSP00000368119.3:n.82+148C>A
ENST00000450095.6:c.-121+148C>A	ENSP00000401956.2:n.-121+148C>A
ENST00000465543.6:n.267C>A
ENST00000468099.2:n.154+148C>A
ENST00000472111.5:n.123+148C>A
ENST00000473506.6:c.82+148C>A	ENSP00000432839.2:n.82+148C>A
ENST00000473529.5:n.129+148C>A
ENST00000485531.1:n.75+15C>A
ENST00000487381.5:n.108+148C>A
ENST00000489643.6:n.112+148C>A
ENST00000554085.5:c.82+148C>A	ENSP00000450419.1:n.82+148C>A
ENST00000554139.5:n.135+148C>A
ENST00000554330.5:n.79+67C>A
ENST00000554550.5:c.82+148C>A	ENSP00000451435.1:n.82+148C>A
ENST00000554638.5:n.106+148C>A
ENST00000554897.5:c.82+148C>A	ENSP00000450942.1:n.82+148C>A
ENST00000554944.5:n.112+148C>A
ENST00000555020.5:n.112+148C>A
ENST00000555086.5:n.86+67C>A
ENST00000555214.5:n.91+148C>A
ENST00000556157.1:n.35C>A
ENST00000556278.1:c.82+148C>A	ENSP00000451792.1:n.82+148C>A
ENST00000556403.5:n.95+67C>A
ENST00000556494.5:n.114+15C>A
ENST00000557541.5:n.275+15C>A
ENST00000557706.5:n.42C>A
ENST00000605275.1:n.466C>A
NM_000155.3:c.82+148C>A	NP_000146.2:n.82+148C>A
NM_001258332.1:c.-121+148C>A	NP_001245261.1:n.-121+148C>A
NM_000155.4:c.82+148C>A MANE Select	NP_000146.2:n.82+148C>A
NM_001258332.2:c.-121+148C>A	NP_001245261.1:n.-121+148C>A