Canonical Allele Identifier: CA2689808627

Gene: GALT

Linked Data

• gnomAD v4: 9-34647604-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647604G>C , CM000671.2:g.34647604G>C	GRCh38
NC_000009.11:g.34647601G>C , CM000671.1:g.34647601G>C	GRCh37
NC_000009.10:g.34637601G>C	NCBI36
NG_009029.1:g.5967G>C
NG_028966.1:g.420G>C
NG_009029.2:g.6016G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.328+37G>C	ENSP00000509954.1:n.328+37G>C
ENST00000378842.8:c.328+37G>C MANE Select	ENSP00000368119.4:n.328+37G>C
ENST00000378842.7:c.328+37G>C	ENSP00000368119.3:n.328+37G>C
ENST00000450095.6:c.51-228G>C	ENSP00000401956.2:n.51-228G>C
ENST00000465543.6:n.667+37G>C
ENST00000472111.5:n.406G>C
ENST00000473506.6:c.279+37G>C	ENSP00000432839.2:n.279+37G>C
ENST00000473529.5:n.412G>C
ENST00000485531.1:n.591G>C
ENST00000487381.5:n.587+37G>C
ENST00000489643.6:n.282+346G>C
ENST00000554085.5:c.*72+37G>C	ENSP00000450419.1:n.*72+37G>C
ENST00000554139.5:n.381+37G>C
ENST00000554330.5:n.313G>C
ENST00000554550.5:c.253-228G>C	ENSP00000451435.1:n.253-228G>C
ENST00000554638.5:n.622G>C
ENST00000554897.5:c.253-228G>C	ENSP00000450942.1:n.253-228G>C
ENST00000554944.5:n.346G>C
ENST00000555020.5:n.358+37G>C
ENST00000555086.5:n.332+37G>C
ENST00000555214.5:n.261+346G>C
ENST00000556157.1:n.452+37G>C
ENST00000556244.1:c.315+37G>C
ENST00000556278.1:c.252+346G>C	ENSP00000451792.1:n.252+346G>C
ENST00000556403.5:n.378G>C
ENST00000556494.5:n.397G>C
ENST00000557541.5:n.472+37G>C
ENST00000557706.5:n.712G>C
NM_000155.3:c.328+37G>C	NP_000146.2:n.328+37G>C
NM_001258332.1:c.51-228G>C	NP_001245261.1:n.51-228G>C
NM_000155.4:c.328+37G>C MANE Select	NP_000146.2:n.328+37G>C
NM_001258332.2:c.51-228G>C	NP_001245261.1:n.51-228G>C