Canonical Allele Identifier: CA373266624
Gene: DNAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517351A>C , CM000671.2:g.34517351A>C GRCh38
NC_000009.11:g.34517349A>C , CM000671.1:g.34517349A>C GRCh37
NC_000009.10:g.34507349A>C NCBI36
NG_008127.1:g.63539A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1885A>C MANE Select ENSP00000242317.4:p.Lys629Gln
ENST00000242317.8:c.1885A>C ENSP00000242317.4:p.Lys629Gln
ENST00000442556.1:c.329+2612A>C
ENST00000470169.5:c.673A>C
ENST00000485580.1:n.461A>C
ENST00000614641.4:c.1897A>C ENSP00000480538.1:p.Lys633Gln
NM_001281428.1:c.1897A>C NP_001268357.1:p.Lys633Gln
NM_012144.3:c.1885A>C NP_036276.1:p.Lys629Gln
XM_006716758.2:c.1354A>C XP_006716821.1:p.Lys452Gln
XM_011517848.1:c.1639A>C XP_011516150.1:p.Lys547Gln
XM_006716758.3:c.1354A>C XP_006716821.1:p.Lys452Gln
XM_011517848.2:c.1639A>C XP_011516150.1:p.Lys547Gln
XM_017014625.2:c.1627A>C XP_016870114.1:p.Lys543Gln
XR_002956774.1:n.1988A>C
NM_012144.4:c.1885A>C MANE Select NP_036276.1:p.Lys629Gln
NM_001281428.2:c.1897A>C NP_001268357.1:p.Lys633Gln