Canonical Allele Identifier: CA2689808459

Gene: GALT

Linked Data

• gnomAD v4: 9-34646881-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646881T>C , CM000671.2:g.34646881T>C	GRCh38
NC_000009.11:g.34646878T>C , CM000671.1:g.34646878T>C	GRCh37
NC_000009.10:g.34636878T>C	NCBI36
NG_009029.1:g.5244T>C
NG_009029.2:g.5293T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.82+95T>C	ENSP00000509954.1:n.82+95T>C
ENST00000378842.8:c.82+95T>C MANE Select	ENSP00000368119.4:n.82+95T>C
ENST00000378842.7:c.82+95T>C	ENSP00000368119.3:n.82+95T>C
ENST00000450095.6:c.-121+95T>C	ENSP00000401956.2:n.-121+95T>C
ENST00000465543.6:n.214T>C
ENST00000468099.2:n.154+95T>C
ENST00000472111.5:n.123+95T>C
ENST00000473506.6:c.82+95T>C	ENSP00000432839.2:n.82+95T>C
ENST00000473529.5:n.129+95T>C
ENST00000485531.1:n.37T>C
ENST00000487381.5:n.108+95T>C
ENST00000489643.6:n.112+95T>C
ENST00000554085.5:c.82+95T>C	ENSP00000450419.1:n.82+95T>C
ENST00000554139.5:n.135+95T>C
ENST00000554330.5:n.79+14T>C
ENST00000554550.5:c.82+95T>C	ENSP00000451435.1:n.82+95T>C
ENST00000554638.5:n.106+95T>C
ENST00000554897.5:c.82+95T>C	ENSP00000450942.1:n.82+95T>C
ENST00000554944.5:n.112+95T>C
ENST00000555020.5:n.112+95T>C
ENST00000555086.5:n.86+14T>C
ENST00000555214.5:n.91+95T>C
ENST00000556278.1:c.82+95T>C	ENSP00000451792.1:n.82+95T>C
ENST00000556403.5:n.95+14T>C
ENST00000556494.5:n.76T>C
ENST00000557541.5:n.237T>C
ENST00000605275.1:n.413T>C
NM_000155.3:c.82+95T>C	NP_000146.2:n.82+95T>C
NM_001258332.1:c.-121+95T>C	NP_001245261.1:n.-121+95T>C
NM_000155.4:c.82+95T>C MANE Select	NP_000146.2:n.82+95T>C
NM_001258332.2:c.-121+95T>C	NP_001245261.1:n.-121+95T>C