Canonical Allele Identifier: CA2274958342
Gene: DNAI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74301079C= , CM000679.2:g.74301079C= GRCh38
NC_000017.10:g.72297218C= , CM000679.1:g.72297218C= GRCh37
NC_000017.9:g.69808813C= NCBI36
NG_016865.1:g.31833C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311014.11:c.898C= MANE Select ENSP00000308312.6:p.Pro300=
ENST00000311014.10:c.898C= ENSP00000308312.6:p.Pro300=
ENST00000446837.2:c.898C= ENSP00000400252.2:p.Pro300=
ENST00000579055.5:c.*269C= ENSP00000462767.1:n.*269C=
ENST00000579490.5:c.1069C= ENSP00000464197.1:p.Pro357=
ENST00000582036.5:c.898C= ENSP00000461950.1:p.Pro300=
NM_001172810.1:c.898C= NP_001166281.1:p.Pro300=
NM_023036.4:c.898C= NP_075462.3:p.Pro300=
XM_011525125.1:c.898C= XP_011523427.1:p.Pro300=
XR_429915.2:n.1020C=
XR_429916.2:n.1020C=
XR_934518.1:n.1022C=
XR_934519.1:n.1019C=
XR_934520.1:n.1095C=
XR_934521.1:n.1007C=
XR_934522.1:n.995C=
XR_934523.1:n.1004C=
XR_934524.1:n.1022C=
XR_934525.1:n.1022C=
XR_934526.1:n.908C=
XR_934527.1:n.1020C=
XR_934528.1:n.1020C=
XR_934529.1:n.901C=
XR_934530.1:n.974C=
XR_934531.1:n.900C=
NM_001172810.2:c.898C= NP_001166281.1:p.Pro300=
NM_001353167.1:c.898C= NP_001340096.1:p.Pro300=
NM_023036.5:c.898C= NP_075462.3:p.Pro300=
NR_148379.1:n.923C=
XM_011525125.2:c.898C= XP_011523427.1:p.Pro300=
XM_024450874.1:c.898C= XP_024306642.1:p.Pro300=
XM_024450875.1:c.898C= XP_024306643.1:p.Pro300=
XM_024450876.1:c.898C= XP_024306644.1:p.Pro300=
XM_024450877.1:c.898C= XP_024306645.1:p.Pro300=
XM_024450878.1:c.898C= XP_024306646.1:p.Pro300=
XM_024450879.1:c.898C= XP_024306647.1:p.Pro300=
XM_024450880.1:c.898C= XP_024306648.1:p.Pro300=
XM_024450881.1:c.784C= XP_024306649.1:p.Pro262=
XM_024450882.1:c.898C= XP_024306650.1:p.Pro300=
XM_024450883.1:c.898C= XP_024306651.1:p.Pro300=
XM_024450884.1:c.898C= XP_024306652.1:p.Pro300=
XM_024450885.1:c.469C= XP_024306653.1:p.Pro157=
XM_024450886.1:c.469C= XP_024306654.1:p.Pro157=
NM_023036.6:c.898C= MANE Select NP_075462.3:p.Pro300=
NM_001172810.3:c.898C= NP_001166281.1:p.Pro300=
NM_001353167.2:c.898C= NP_001340096.1:p.Pro300=
NR_148379.2:n.899C=