Canonical Allele Identifier: CA1845591105
Gene: DNAI1 HGNC NCBI

Linked Data

dbSNP Id: rs1825183717

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517141del , CM000671.2:g.34517141del GRCh38
NC_000009.11:g.34517139del , CM000671.1:g.34517139del GRCh37
NC_000009.10:g.34507139del NCBI36
NG_008127.1:g.63329del

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1819-144del MANE Select ENSP00000242317.4:n.1819-144del
ENST00000242317.8:c.1819-144del ENSP00000242317.4:n.1819-144del
ENST00000442556.1:c.329+2402del
ENST00000470169.5:c.607-144del
ENST00000485580.1:n.395-144del
ENST00000614641.4:c.1831-144del ENSP00000480538.1:n.1831-144del
NM_001281428.1:c.1831-144del NP_001268357.1:n.1831-144del
NM_012144.3:c.1819-144del NP_036276.1:n.1819-144del
XM_006716758.2:c.1288-144del XP_006716821.1:n.1288-144del
XM_011517847.1:c.1831-54del XP_011516149.1:n.1831-54del
XM_011517848.1:c.1573-144del XP_011516150.1:n.1573-144del
XR_929233.1:n.1975-54del
XM_006716758.3:c.1288-144del XP_006716821.1:n.1288-144del
XM_011517847.3:c.1831-54del XP_011516149.1:n.1831-54del
XM_011517848.2:c.1573-144del XP_011516150.1:n.1573-144del
XM_017014625.2:c.1561-144del XP_016870114.1:n.1561-144del
XR_002956774.1:n.1922-144del
XR_929233.2:n.1922-54del
NM_012144.4:c.1819-144del MANE Select NP_036276.1:n.1819-144del
NM_001281428.2:c.1831-144del NP_001268357.1:n.1831-144del