Canonical Allele Identifier: CA1845599290
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34506825_34506828delinsCCTT , CM000671.2:g.34506825_34506828delinsCCTT GRCh38
NC_000009.11:g.34506823_34506826delinsCCTT , CM000671.1:g.34506823_34506826delinsCCTT GRCh37
NC_000009.10:g.34496823_34496826delinsCCTT NCBI36
NG_008127.1:g.53013_53016delinsCCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1262_1265delinsCCTT MANE Select ENSP00000242317.4:p.Ser421=
ENST00000242317.8:c.1262_1265delinsCCTT ENSP00000242317.4:p.Ser421=
ENST00000470169.5:c.199_202delinsCCTT
ENST00000614641.4:c.1274_1277delinsCCTT ENSP00000480538.1:p.Ser425=
NM_001281428.1:c.1274_1277delinsCCTT NP_001268357.1:p.Ser425=
NM_012144.3:c.1262_1265delinsCCTT NP_036276.1:p.Ser421=
XM_006716758.2:c.731_734delinsCCTT XP_006716821.1:p.Ser244=
XM_011517846.1:c.1274_1277delinsCCTT XP_011516148.1:p.Ser425=
XM_011517847.1:c.1274_1277delinsCCTT XP_011516149.1:p.Ser425=
XM_011517848.1:c.1274_1277delinsCCTT XP_011516150.1:p.Ser425=
XM_011517849.1:c.1274_1277delinsCCTT XP_011516151.1:p.Ser425=
XM_011517850.1:c.1274_1277delinsCCTT XP_011516152.1:p.Ser425=
XR_929232.1:n.1528_1531delinsCCTT
XR_929233.1:n.1528_1531delinsCCTT
XR_929235.1:n.1528_1531delinsCCTT
XM_006716758.3:c.731_734delinsCCTT XP_006716821.1:p.Ser244=
XM_011517846.2:c.1274_1277delinsCCTT XP_011516148.1:p.Ser425=
XM_011517847.3:c.1274_1277delinsCCTT XP_011516149.1:p.Ser425=
XM_011517848.2:c.1274_1277delinsCCTT XP_011516150.1:p.Ser425=
XM_011517849.2:c.1274_1277delinsCCTT XP_011516151.1:p.Ser425=
XM_011517850.3:c.1274_1277delinsCCTT XP_011516152.1:p.Ser425=
XM_017014625.2:c.1262_1265delinsCCTT XP_016870114.1:p.Ser421=
XR_002956774.1:n.1475_1478delinsCCTT
XR_929232.2:n.1475_1478delinsCCTT
XR_929233.2:n.1475_1478delinsCCTT
NM_012144.4:c.1262_1265delinsCCTT MANE Select NP_036276.1:p.Ser421=
NM_001281428.2:c.1274_1277delinsCCTT NP_001268357.1:p.Ser425=