Canonical Allele Identifier: CA1845592501
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517485T= , CM000671.2:g.34517485T= GRCh38
NC_000009.11:g.34517483T= , CM000671.1:g.34517483T= GRCh37
NC_000009.10:g.34507483T= NCBI36
NG_008127.1:g.63673T=

Transcript Alleles

HGVS Amino-acid change
ENST00000242317.9:c.2001+18T= MANE Select ENSP00000242317.4:n.2001+18T=
ENST00000242317.8:c.2001+18T= ENSP00000242317.4:n.2001+18T=
ENST00000442556.1:c.329+2746T=
ENST00000614641.4:c.2013+18T= ENSP00000480538.1:n.2013+18T=
NM_001281428.1:c.2013+18T= NP_001268357.1:n.2013+18T=
NM_012144.3:c.2001+18T= NP_036276.1:n.2001+18T=
XM_006716758.2:c.1470+18T= XP_006716821.1:n.1470+18T=
XM_011517848.1:c.1755+18T= XP_011516150.1:n.1755+18T=
XM_006716758.3:c.1470+18T= XP_006716821.1:n.1470+18T=
XM_011517848.2:c.1755+18T= XP_011516150.1:n.1755+18T=
XM_017014625.2:c.1743+18T= XP_016870114.1:n.1743+18T=
XR_002956774.1:n.2104+18T=
NM_012144.4:c.2001+18T= MANE Select NP_036276.1:n.2001+18T=
NM_001281428.2:c.2013+18T= NP_001268357.1:n.2013+18T=