Canonical Allele Identifier: CA587243842

Gene: GALT

Linked Data

• dbSNP Id: rs1433474228
• gnomAD v2: 9-34646853-T-C
• gnomAD v4: 9-34646856-T-C
• MyVariant Identifiers: chr9:g.34646853T>C (hg19) ; chr9:g.34646856T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646856T>C , CM000671.2:g.34646856T>C	GRCh38
NC_000009.11:g.34646853T>C , CM000671.1:g.34646853T>C	GRCh37
NC_000009.10:g.34636853T>C	NCBI36
NG_009029.1:g.5219T>C
NG_009029.2:g.5268T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.82+70T>C	ENSP00000509954.1:n.82+70T>C
ENST00000378842.8:c.82+70T>C MANE Select	ENSP00000368119.4:n.82+70T>C
ENST00000378842.7:c.82+70T>C	ENSP00000368119.3:n.82+70T>C
ENST00000450095.6:c.-121+70T>C	ENSP00000401956.2:n.-121+70T>C
ENST00000465543.6:n.189T>C
ENST00000468099.2:n.154+70T>C
ENST00000472111.5:n.123+70T>C
ENST00000473506.6:c.82+70T>C	ENSP00000432839.2:n.82+70T>C
ENST00000473529.5:n.129+70T>C
ENST00000485531.1:n.12T>C
ENST00000487381.5:n.108+70T>C
ENST00000489643.6:n.112+70T>C
ENST00000554085.5:c.82+70T>C	ENSP00000450419.1:n.82+70T>C
ENST00000554139.5:n.135+70T>C
ENST00000554330.5:n.68T>C
ENST00000554550.5:c.82+70T>C	ENSP00000451435.1:n.82+70T>C
ENST00000554638.5:n.106+70T>C
ENST00000554897.5:c.82+70T>C	ENSP00000450942.1:n.82+70T>C
ENST00000554944.5:n.112+70T>C
ENST00000555020.5:n.112+70T>C
ENST00000555086.5:n.75T>C
ENST00000555214.5:n.91+70T>C
ENST00000556278.1:c.82+70T>C	ENSP00000451792.1:n.82+70T>C
ENST00000556403.5:n.84T>C
ENST00000556494.5:n.51T>C
ENST00000557541.5:n.212T>C
ENST00000605275.1:n.388T>C
NM_000155.3:c.82+70T>C	NP_000146.2:n.82+70T>C
NM_001258332.1:c.-121+70T>C	NP_001245261.1:n.-121+70T>C
NM_000155.4:c.82+70T>C MANE Select	NP_000146.2:n.82+70T>C
NM_001258332.2:c.-121+70T>C	NP_001245261.1:n.-121+70T>C