Canonical Allele Identifier: CA1845591376
Gene: DNAI1 HGNC NCBI

Linked Data

dbSNP Id: rs1425020976
gnomAD v4: 9-34517248-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517248A>G , CM000671.2:g.34517248A>G GRCh38
NC_000009.11:g.34517246A>G , CM000671.1:g.34517246A>G GRCh37
NC_000009.10:g.34507246A>G NCBI36
NG_008127.1:g.63436A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1819-37A>G MANE Select ENSP00000242317.4:n.1819-37A>G
ENST00000242317.8:c.1819-37A>G ENSP00000242317.4:n.1819-37A>G
ENST00000442556.1:c.329+2509A>G
ENST00000470169.5:c.607-37A>G
ENST00000485580.1:n.395-37A>G
ENST00000614641.4:c.1831-37A>G ENSP00000480538.1:n.1831-37A>G
NM_001281428.1:c.1831-37A>G NP_001268357.1:n.1831-37A>G
NM_012144.3:c.1819-37A>G NP_036276.1:n.1819-37A>G
XM_006716758.2:c.1288-37A>G XP_006716821.1:n.1288-37A>G
XM_011517847.1:c.*18A>G XP_011516149.1:n.*18A>G
XM_011517848.1:c.1573-37A>G XP_011516150.1:n.1573-37A>G
XR_929233.1:n.2028A>G
XM_006716758.3:c.1288-37A>G XP_006716821.1:n.1288-37A>G
XM_011517847.3:c.*18A>G XP_011516149.1:n.*18A>G
XM_011517848.2:c.1573-37A>G XP_011516150.1:n.1573-37A>G
XM_017014625.2:c.1561-37A>G XP_016870114.1:n.1561-37A>G
XR_002956774.1:n.1922-37A>G
XR_929233.2:n.1975A>G
NM_012144.4:c.1819-37A>G MANE Select NP_036276.1:n.1819-37A>G
NM_001281428.2:c.1831-37A>G NP_001268357.1:n.1831-37A>G