Canonical Allele Identifier: CA373266468
Gene: DNAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517319A>G , CM000671.2:g.34517319A>G GRCh38
NC_000009.11:g.34517317A>G , CM000671.1:g.34517317A>G GRCh37
NC_000009.10:g.34507317A>G NCBI36
NG_008127.1:g.63507A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1853A>G MANE Select ENSP00000242317.4:p.Glu618Gly
ENST00000242317.8:c.1853A>G ENSP00000242317.4:p.Glu618Gly
ENST00000442556.1:c.329+2580A>G
ENST00000470169.5:c.641A>G
ENST00000485580.1:n.429A>G
ENST00000614641.4:c.1865A>G ENSP00000480538.1:p.Glu622Gly
NM_001281428.1:c.1865A>G NP_001268357.1:p.Glu622Gly
NM_012144.3:c.1853A>G NP_036276.1:p.Glu618Gly
XM_006716758.2:c.1322A>G XP_006716821.1:p.Glu441Gly
XM_011517848.1:c.1607A>G XP_011516150.1:p.Glu536Gly
XM_006716758.3:c.1322A>G XP_006716821.1:p.Glu441Gly
XM_011517848.2:c.1607A>G XP_011516150.1:p.Glu536Gly
XM_017014625.2:c.1595A>G XP_016870114.1:p.Glu532Gly
XR_002956774.1:n.1956A>G
NM_012144.4:c.1853A>G MANE Select NP_036276.1:p.Glu618Gly
NM_001281428.2:c.1865A>G NP_001268357.1:p.Glu622Gly