Canonical Allele Identifier: CA2238455815
Gene: DNAAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84149074G= , CM000678.2:g.84149074G= GRCh38
NC_000016.9:g.84182679G= , CM000678.1:g.84182679G= GRCh37
NC_000016.8:g.82740180G= NCBI36
NG_021174.1:g.8815G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378553.10:c.192G= MANE Select ENSP00000367815.5:p.Gln64=
ENST00000378553.9:c.192G= ENSP00000367815.5:p.Gln64=
ENST00000563093.5:c.192G= ENSP00000457373.1:p.Gln64=
ENST00000567918.5:c.192G= ENSP00000455154.1:p.Gln64=
ENST00000570298.5:n.346G=
NM_178452.4:c.192G= NP_848547.4:p.Gln64=
XM_006721129.1:c.192G= XP_006721192.1:p.Gln64=
XM_011522850.1:c.192G= XP_011521152.1:p.Gln64=
XM_011522851.1:c.192G= XP_011521153.1:p.Gln64=
XM_011522852.1:c.192G= XP_011521154.1:p.Gln64=
XM_011522853.1:c.192G= XP_011521155.1:p.Gln64=
XM_011522854.1:c.192G= XP_011521156.1:p.Gln64=
XM_011522855.1:c.192G= XP_011521157.1:p.Gln64=
XM_011522856.1:c.-70G= XP_011521158.1:n.-70G=
XM_011522857.1:c.192G= XP_011521159.1:p.Gln64=
XM_011522858.1:c.192G= XP_011521160.1:p.Gln64=
NM_178452.5:c.192G= NP_848547.4:p.Gln64=
XM_006721129.3:c.192G= XP_006721192.1:p.Gln64=
XM_011522853.3:c.192G= XP_011521155.1:p.Gln64=
XM_011522854.3:c.192G= XP_011521156.1:p.Gln64=
XM_011522855.3:c.192G= XP_011521157.1:p.Gln64=
XM_011522857.3:c.192G= XP_011521159.1:p.Gln64=
XM_011522858.3:c.192G= XP_011521160.1:p.Gln64=
XM_017022918.2:c.192G= XP_016878407.1:p.Gln64=
XM_017022919.1:c.-70G= XP_016878408.1:n.-70G=
XR_001751829.2:n.366G=
XR_001751830.2:n.366G=
XR_001751831.2:n.366G=
XR_001751832.1:n.675G=
NM_178452.6:c.192G= MANE Select NP_848547.4:p.Gln64=