Canonical Allele Identifier: CA1123116700
Gene: DNAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517262_34517263insACG , CM000671.2:g.34517262_34517263insACG GRCh38
NC_000009.11:g.34517260_34517261insACG , CM000671.1:g.34517260_34517261insACG GRCh37
NC_000009.10:g.34507260_34507261insACG NCBI36
NG_008127.1:g.63450_63451insACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1819-23_1819-22insACG MANE Select ENSP00000242317.4:n.1819-23_1819-22insACG
ENST00000242317.8:c.1819-23_1819-22insACG ENSP00000242317.4:n.1819-23_1819-22insACG
ENST00000442556.1:c.329+2523_329+2524insACG
ENST00000470169.5:c.607-23_607-22insACG
ENST00000485580.1:n.395-23_395-22insACG
ENST00000614641.4:c.1831-23_1831-22insACG ENSP00000480538.1:n.1831-23_1831-22insACG
NM_001281428.1:c.1831-23_1831-22insACG NP_001268357.1:n.1831-23_1831-22insACG
NM_012144.3:c.1819-23_1819-22insACG NP_036276.1:n.1819-23_1819-22insACG
XM_006716758.2:c.1288-23_1288-22insACG XP_006716821.1:n.1288-23_1288-22insACG
XM_011517847.1:c.*32_*33insACG XP_011516149.1:n.*32_*33insACG
XM_011517848.1:c.1573-23_1573-22insACG XP_011516150.1:n.1573-23_1573-22insACG
XR_929233.1:n.2042_2043insACG
XM_006716758.3:c.1288-23_1288-22insACG XP_006716821.1:n.1288-23_1288-22insACG
XM_011517847.3:c.*32_*33insACG XP_011516149.1:n.*32_*33insACG
XM_011517848.2:c.1573-23_1573-22insACG XP_011516150.1:n.1573-23_1573-22insACG
XM_017014625.2:c.1561-23_1561-22insACG XP_016870114.1:n.1561-23_1561-22insACG
XR_002956774.1:n.1922-23_1922-22insACG
XR_929233.2:n.1989_1990insACG
NM_012144.4:c.1819-23_1819-22insACG MANE Select NP_036276.1:n.1819-23_1819-22insACG
NM_001281428.2:c.1831-23_1831-22insACG NP_001268357.1:n.1831-23_1831-22insACG