Canonical Allele Identifier: CA2579327434
Gene: DNAI1 HGNC NCBI

Linked Data

gnomAD v4: 9-34513013-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34513013C>G , CM000671.2:g.34513013C>G GRCh38
NC_000009.11:g.34513011C>G , CM000671.1:g.34513011C>G GRCh37
NC_000009.10:g.34503011C>G NCBI36
NG_008127.1:g.59201C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1490-99C>G MANE Select ENSP00000242317.4:n.1490-99C>G
ENST00000242317.8:c.1490-99C>G ENSP00000242317.4:n.1490-99C>G
ENST00000470169.5:c.427-99C>G
ENST00000614641.4:c.1502-99C>G ENSP00000480538.1:n.1502-99C>G
NM_001281428.1:c.1502-99C>G NP_001268357.1:n.1502-99C>G
NM_012144.3:c.1490-99C>G NP_036276.1:n.1490-99C>G
XM_006716758.2:c.959-99C>G XP_006716821.1:n.959-99C>G
XM_011517846.1:c.1502-99C>G XP_011516148.1:n.1502-99C>G
XM_011517847.1:c.1502-99C>G XP_011516149.1:n.1502-99C>G
XM_011517848.1:c.1324-1381C>G XP_011516150.1:n.1324-1381C>G
XM_011517849.1:c.1502-99C>G XP_011516151.1:n.1502-99C>G
XR_929232.1:n.1756-99C>G
XR_929233.1:n.1756-99C>G
XR_929235.1:n.1578-1491C>G
XM_006716758.3:c.959-99C>G XP_006716821.1:n.959-99C>G
XM_011517846.2:c.1502-99C>G XP_011516148.1:n.1502-99C>G
XM_011517847.3:c.1502-99C>G XP_011516149.1:n.1502-99C>G
XM_011517848.2:c.1324-1381C>G XP_011516150.1:n.1324-1381C>G
XM_011517849.2:c.1502-99C>G XP_011516151.1:n.1502-99C>G
XM_017014625.2:c.1312-1381C>G XP_016870114.1:n.1312-1381C>G
XR_002956774.1:n.1703-99C>G
XR_929232.2:n.1703-99C>G
XR_929233.2:n.1703-99C>G
NM_012144.4:c.1490-99C>G MANE Select NP_036276.1:n.1490-99C>G
NM_001281428.2:c.1502-99C>G NP_001268357.1:n.1502-99C>G