Canonical Allele Identifier: CA373266609
Gene: DNAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517349A>G , CM000671.2:g.34517349A>G GRCh38
NC_000009.11:g.34517347A>G , CM000671.1:g.34517347A>G GRCh37
NC_000009.10:g.34507347A>G NCBI36
NG_008127.1:g.63537A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1883A>G MANE Select ENSP00000242317.4:p.Lys628Arg
ENST00000242317.8:c.1883A>G ENSP00000242317.4:p.Lys628Arg
ENST00000442556.1:c.329+2610A>G
ENST00000470169.5:c.671A>G
ENST00000485580.1:n.459A>G
ENST00000614641.4:c.1895A>G ENSP00000480538.1:p.Lys632Arg
NM_001281428.1:c.1895A>G NP_001268357.1:p.Lys632Arg
NM_012144.3:c.1883A>G NP_036276.1:p.Lys628Arg
XM_006716758.2:c.1352A>G XP_006716821.1:p.Lys451Arg
XM_011517848.1:c.1637A>G XP_011516150.1:p.Lys546Arg
XM_006716758.3:c.1352A>G XP_006716821.1:p.Lys451Arg
XM_011517848.2:c.1637A>G XP_011516150.1:p.Lys546Arg
XM_017014625.2:c.1625A>G XP_016870114.1:p.Lys542Arg
XR_002956774.1:n.1986A>G
NM_012144.4:c.1883A>G MANE Select NP_036276.1:p.Lys628Arg
NM_001281428.2:c.1895A>G NP_001268357.1:p.Lys632Arg