Canonical Allele Identifier: CA2689809674

Gene: GALT

Linked Data

• gnomAD v4: 9-34648899-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648899_34648900insC , CM000671.2:g.34648899_34648900insC	GRCh38
NC_000009.11:g.34648896_34648897insC , CM000671.1:g.34648896_34648897insC	GRCh37
NC_000009.10:g.34638896_34638897insC	NCBI36
NG_009029.1:g.7262_7263insC
NG_028966.1:g.1715_1716insC
NG_009029.2:g.7311_7312insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*408+5_*408+6insC	ENSP00000509954.1:n.*408+5_*408+6insC
ENST00000378842.8:c.820+5_820+6insC MANE Select	ENSP00000368119.4:n.820+5_820+6insC
ENST00000378842.7:c.820+5_820+6insC	ENSP00000368119.3:n.820+5_820+6insC
ENST00000450095.6:c.493+5_493+6insC	ENSP00000401956.2:n.493+5_493+6insC
ENST00000489643.6:n.900+5_900+6insC
ENST00000554085.5:c.*564+5_*564+6insC	ENSP00000450419.1:n.*564+5_*564+6insC
ENST00000554550.5:c.*440+5_*440+6insC	ENSP00000451435.1:n.*440+5_*440+6insC
ENST00000554638.5:n.1292+5_1292+6insC
ENST00000555020.5:n.1281+5_1281+6insC
ENST00000555086.5:n.829_830insC
ENST00000555754.1:n.170_171insC
ENST00000556278.1:c.432+443_432+444insC	ENSP00000451792.1:n.432+443_432+444insC
ENST00000557706.5:n.1387_1388insC
NM_000155.3:c.820+5_820+6insC	NP_000146.2:n.820+5_820+6insC
NM_001258332.1:c.493+5_493+6insC	NP_001245261.1:n.493+5_493+6insC
NM_000155.4:c.820+5_820+6insC MANE Select	NP_000146.2:n.820+5_820+6insC
NM_001258332.2:c.493+5_493+6insC	NP_001245261.1:n.493+5_493+6insC