Canonical Allele Identifier: CA2274958345
Gene: DNAI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74301082A= , CM000679.2:g.74301082A= GRCh38
NC_000017.10:g.72297221A= , CM000679.1:g.72297221A= GRCh37
NC_000017.9:g.69808816A= NCBI36
NG_016865.1:g.31836A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311014.11:c.901A= MANE Select ENSP00000308312.6:p.Thr301=
ENST00000311014.10:c.901A= ENSP00000308312.6:p.Thr301=
ENST00000446837.2:c.901A= ENSP00000400252.2:p.Thr301=
ENST00000579055.5:c.*272A= ENSP00000462767.1:n.*272A=
ENST00000579490.5:c.1072A= ENSP00000464197.1:p.Thr358=
ENST00000582036.5:c.901A= ENSP00000461950.1:p.Thr301=
NM_001172810.1:c.901A= NP_001166281.1:p.Thr301=
NM_023036.4:c.901A= NP_075462.3:p.Thr301=
XM_011525125.1:c.901A= XP_011523427.1:p.Thr301=
XR_429915.2:n.1023A=
XR_429916.2:n.1023A=
XR_934518.1:n.1025A=
XR_934519.1:n.1022A=
XR_934520.1:n.1098A=
XR_934521.1:n.1010A=
XR_934522.1:n.998A=
XR_934523.1:n.1007A=
XR_934524.1:n.1025A=
XR_934525.1:n.1025A=
XR_934526.1:n.911A=
XR_934527.1:n.1023A=
XR_934528.1:n.1023A=
XR_934529.1:n.904A=
XR_934530.1:n.977A=
XR_934531.1:n.903A=
NM_001172810.2:c.901A= NP_001166281.1:p.Thr301=
NM_001353167.1:c.901A= NP_001340096.1:p.Thr301=
NM_023036.5:c.901A= NP_075462.3:p.Thr301=
NR_148379.1:n.926A=
XM_011525125.2:c.901A= XP_011523427.1:p.Thr301=
XM_024450874.1:c.901A= XP_024306642.1:p.Thr301=
XM_024450875.1:c.901A= XP_024306643.1:p.Thr301=
XM_024450876.1:c.901A= XP_024306644.1:p.Thr301=
XM_024450877.1:c.901A= XP_024306645.1:p.Thr301=
XM_024450878.1:c.901A= XP_024306646.1:p.Thr301=
XM_024450879.1:c.901A= XP_024306647.1:p.Thr301=
XM_024450880.1:c.901A= XP_024306648.1:p.Thr301=
XM_024450881.1:c.787A= XP_024306649.1:p.Thr263=
XM_024450882.1:c.901A= XP_024306650.1:p.Thr301=
XM_024450883.1:c.901A= XP_024306651.1:p.Thr301=
XM_024450884.1:c.901A= XP_024306652.1:p.Thr301=
XM_024450885.1:c.472A= XP_024306653.1:p.Thr158=
XM_024450886.1:c.472A= XP_024306654.1:p.Thr158=
NM_023036.6:c.901A= MANE Select NP_075462.3:p.Thr301=
NM_001172810.3:c.901A= NP_001166281.1:p.Thr301=
NM_001353167.2:c.901A= NP_001340096.1:p.Thr301=
NR_148379.2:n.902A=