Canonical Allele Identifier: CA1123150632
Gene: DNAI1 HGNC NCBI

Linked Data

dbSNP Id: rs953709288
gnomAD v3: 9-34489266-A-T
gnomAD v4: 9-34489266-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34489266A>T , CM000671.2:g.34489266A>T GRCh38
NC_000009.11:g.34489264A>T , CM000671.1:g.34489264A>T GRCh37
NC_000009.10:g.34479264A>T NCBI36
NG_008127.1:g.35454A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000242317.9:c.262-57A>T MANE Select ENSP00000242317.4:n.262-57A>T
ENST00000242317.8:c.262-57A>T ENSP00000242317.4:n.262-57A>T
ENST00000437363.5:c.229-57A>T ENSP00000395396.1:n.229-57A>T
ENST00000488369.1:n.378-57A>T
ENST00000614641.4:c.262-57A>T ENSP00000480538.1:n.262-57A>T
NM_001281428.1:c.262-57A>T NP_001268357.1:n.262-57A>T
NM_012144.3:c.262-57A>T NP_036276.1:n.262-57A>T
XM_011517846.1:c.262-57A>T XP_011516148.1:n.262-57A>T
XM_011517847.1:c.262-57A>T XP_011516149.1:n.262-57A>T
XM_011517848.1:c.262-57A>T XP_011516150.1:n.262-57A>T
XM_011517849.1:c.262-57A>T XP_011516151.1:n.262-57A>T
XM_011517850.1:c.262-57A>T XP_011516152.1:n.262-57A>T
XR_929232.1:n.516-57A>T
XR_929233.1:n.516-57A>T
XR_929235.1:n.516-57A>T
XM_006716758.3:c.-215-57A>T XP_006716821.1:n.-215-57A>T
XM_011517846.2:c.262-57A>T XP_011516148.1:n.262-57A>T
XM_011517847.3:c.262-57A>T XP_011516149.1:n.262-57A>T
XM_011517848.2:c.262-57A>T XP_011516150.1:n.262-57A>T
XM_011517849.2:c.262-57A>T XP_011516151.1:n.262-57A>T
XM_011517850.3:c.262-57A>T XP_011516152.1:n.262-57A>T
XM_017014625.2:c.262-57A>T XP_016870114.1:n.262-57A>T
XR_002956774.1:n.463-57A>T
XR_929232.2:n.463-57A>T
XR_929233.2:n.463-57A>T
NM_012144.4:c.262-57A>T MANE Select NP_036276.1:n.262-57A>T
NM_001281428.2:c.262-57A>T NP_001268357.1:n.262-57A>T