Canonical Allele Identifier: CA2689810801

Gene: GALT

Linked Data

• gnomAD v4: 9-34649374-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649382_34649383del , CM000671.2:g.34649382_34649383del	GRCh38
NC_000009.11:g.34649379_34649380del , CM000671.1:g.34649379_34649380del	GRCh37
NC_000009.10:g.34639379_34639380del	NCBI36
NG_009029.1:g.7745_7746del
NG_028966.1:g.2198_2199del
NG_009029.2:g.7794_7795del

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*493-28_*493-27del	ENSP00000509954.1:n.*493-28_*493-27del
ENST00000378842.8:c.905-28_905-27del MANE Select	ENSP00000368119.4:n.905-28_905-27del
ENST00000378842.7:c.905-28_905-27del	ENSP00000368119.3:n.905-28_905-27del
ENST00000450095.6:c.578-28_578-27del	ENSP00000401956.2:n.578-28_578-27del
ENST00000488412.2:n.461_462del
ENST00000489643.6:n.1285_1286del
ENST00000554550.5:c.*525-28_*525-27del	ENSP00000451435.1:n.*525-28_*525-27del
ENST00000554638.5:n.1377-28_1377-27del
ENST00000555020.5:n.1666_1667del
ENST00000555754.1:n.353-28_353-27del
ENST00000556278.1:c.432+926_432+927del	ENSP00000451792.1:n.432+926_432+927del
ENST00000557706.5:n.1480-28_1480-27del
NM_000155.3:c.905-28_905-27del	NP_000146.2:n.905-28_905-27del
NM_001258332.1:c.578-28_578-27del	NP_001245261.1:n.578-28_578-27del
NM_000155.4:c.905-28_905-27del MANE Select	NP_000146.2:n.905-28_905-27del
NM_001258332.2:c.578-28_578-27del	NP_001245261.1:n.578-28_578-27del