Canonical Allele Identifier: CA5034555
Gene: DNAI1 HGNC NCBI

Linked Data

dbSNP Id: rs761565342

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517255dup , CM000671.2:g.34517255dup GRCh38
NC_000009.11:g.34517253dup , CM000671.1:g.34517253dup GRCh37
NC_000009.10:g.34507253dup NCBI36
NG_008127.1:g.63443dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1819-30dup MANE Select ENSP00000242317.4:n.1819-30dup
ENST00000242317.8:c.1819-30dup ENSP00000242317.4:n.1819-30dup
ENST00000442556.1:c.329+2516dup
ENST00000470169.5:c.607-30dup
ENST00000485580.1:n.395-30dup
ENST00000614641.4:c.1831-30dup ENSP00000480538.1:n.1831-30dup
NM_001281428.1:c.1831-30dup NP_001268357.1:n.1831-30dup
NM_012144.3:c.1819-30dup NP_036276.1:n.1819-30dup
XM_006716758.2:c.1288-30dup XP_006716821.1:n.1288-30dup
XM_011517847.1:c.*25dup XP_011516149.1:n.*25dup
XM_011517848.1:c.1573-30dup XP_011516150.1:n.1573-30dup
XR_929233.1:n.2035dup
XM_006716758.3:c.1288-30dup XP_006716821.1:n.1288-30dup
XM_011517847.3:c.*25dup XP_011516149.1:n.*25dup
XM_011517848.2:c.1573-30dup XP_011516150.1:n.1573-30dup
XM_017014625.2:c.1561-30dup XP_016870114.1:n.1561-30dup
XR_002956774.1:n.1922-30dup
XR_929233.2:n.1982dup
NM_012144.4:c.1819-30dup MANE Select NP_036276.1:n.1819-30dup
NM_001281428.2:c.1831-30dup NP_001268357.1:n.1831-30dup