Canonical Allele Identifier: CA1845574913
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34489454_34489459delinsGACTCT , CM000671.2:g.34489454_34489459delinsGACTCT GRCh38
NC_000009.11:g.34489452_34489457delinsGACTCT , CM000671.1:g.34489452_34489457delinsGACTCT GRCh37
NC_000009.10:g.34479452_34479457delinsGACTCT NCBI36
NG_008127.1:g.35642_35647delinsGACTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.388+5_388+10delinsGACTCT MANE Select ENSP00000242317.4:n.388+5_388+10delinsGACTCT
ENST00000242317.8:c.388+5_388+10delinsGACTCT ENSP00000242317.4:n.388+5_388+10delinsGACTCT
ENST00000437363.5:c.355+5_355+10delinsGACTCT ENSP00000395396.1:n.355+5_355+10delinsGACTCT
ENST00000488369.1:n.504+5_504+10delinsGACTCT
ENST00000614641.4:c.388+5_388+10delinsGACTCT ENSP00000480538.1:n.388+5_388+10delinsGACTCT
NM_001281428.1:c.388+5_388+10delinsGACTCT NP_001268357.1:n.388+5_388+10delinsGACTCT
NM_012144.3:c.388+5_388+10delinsGACTCT NP_036276.1:n.388+5_388+10delinsGACTCT
XM_011517846.1:c.388+5_388+10delinsGACTCT XP_011516148.1:n.388+5_388+10delinsGACTCT
XM_011517847.1:c.388+5_388+10delinsGACTCT XP_011516149.1:n.388+5_388+10delinsGACTCT
XM_011517848.1:c.388+5_388+10delinsGACTCT XP_011516150.1:n.388+5_388+10delinsGACTCT
XM_011517849.1:c.388+5_388+10delinsGACTCT XP_011516151.1:n.388+5_388+10delinsGACTCT
XM_011517850.1:c.388+5_388+10delinsGACTCT XP_011516152.1:n.388+5_388+10delinsGACTCT
XR_929232.1:n.642+5_642+10delinsGACTCT
XR_929233.1:n.642+5_642+10delinsGACTCT
XR_929235.1:n.642+5_642+10delinsGACTCT
XM_006716758.3:c.-89+5_-89+10delinsGACTCT XP_006716821.1:n.-89+5_-89+10delinsGACTCT
XM_011517846.2:c.388+5_388+10delinsGACTCT XP_011516148.1:n.388+5_388+10delinsGACTCT
XM_011517847.3:c.388+5_388+10delinsGACTCT XP_011516149.1:n.388+5_388+10delinsGACTCT
XM_011517848.2:c.388+5_388+10delinsGACTCT XP_011516150.1:n.388+5_388+10delinsGACTCT
XM_011517849.2:c.388+5_388+10delinsGACTCT XP_011516151.1:n.388+5_388+10delinsGACTCT
XM_011517850.3:c.388+5_388+10delinsGACTCT XP_011516152.1:n.388+5_388+10delinsGACTCT
XM_017014625.2:c.388+5_388+10delinsGACTCT XP_016870114.1:n.388+5_388+10delinsGACTCT
XR_002956774.1:n.589+5_589+10delinsGACTCT
XR_929232.2:n.589+5_589+10delinsGACTCT
XR_929233.2:n.589+5_589+10delinsGACTCT
NM_012144.4:c.388+5_388+10delinsGACTCT MANE Select NP_036276.1:n.388+5_388+10delinsGACTCT
NM_001281428.2:c.388+5_388+10delinsGACTCT NP_001268357.1:n.388+5_388+10delinsGACTCT