Canonical Allele Identifier: CA1123157215
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1821157965

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648178del , CM000671.2:g.34648178del GRCh38
NC_000009.11:g.34648175del , CM000671.1:g.34648175del GRCh37
NC_000009.10:g.34638175del NCBI36
NG_009029.1:g.6541del
NG_028966.1:g.994del
NG_009029.2:g.6590del

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*152+7del ENSP00000509954.1:n.*152+7del
ENST00000378842.8:c.564+7del MANE Select ENSP00000368119.4:n.564+7del
ENST00000378842.7:c.564+7del ENSP00000368119.3:n.564+7del
ENST00000450095.6:c.237+7del ENSP00000401956.2:n.237+7del
ENST00000472111.5:n.820+7del
ENST00000473506.6:c.*152+7del ENSP00000432839.2:n.*152+7del
ENST00000473529.5:n.723+7del
ENST00000485531.1:n.1158+7del
ENST00000487381.5:n.949+7del
ENST00000489643.6:n.339+7del
ENST00000554085.5:c.*308+7del ENSP00000450419.1:n.*308+7del
ENST00000554139.5:n.810+7del
ENST00000554550.5:c.*184+7del ENSP00000451435.1:n.*184+7del
ENST00000554638.5:n.1036+7del
ENST00000554897.5:c.*251+7del ENSP00000450942.1:n.*251+7del
ENST00000554944.5:n.913+7del
ENST00000555020.5:n.720+7del
ENST00000555086.5:n.568+7del
ENST00000555214.5:n.385+7del
ENST00000556244.1:c.551+7del
ENST00000556278.1:c.309+7del ENSP00000451792.1:n.309+7del
ENST00000556494.5:n.685+7del
ENST00000557706.5:n.1126+7del
NM_000155.3:c.564+7del NP_000146.2:n.564+7del
NM_001258332.1:c.237+7del NP_001245261.1:n.237+7del
NM_000155.4:c.564+7del MANE Select NP_000146.2:n.564+7del
NM_001258332.2:c.237+7del NP_001245261.1:n.237+7del