Canonical Allele Identifier: CA2238462003

Gene: DNAAF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84159636_84159637delinsCT , CM000678.2:g.84159636_84159637delinsCT	GRCh38
NC_000016.9:g.84193241_84193242delinsCT , CM000678.1:g.84193241_84193242delinsCT	GRCh37
NC_000016.8:g.82750742_82750743delinsCT	NCBI36
NG_021174.1:g.19377_19378delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000378553.10:c.742-39_742-38delinsCT MANE Select	ENSP00000367815.5:n.742-39_742-38delinsCT...
ENST00000378553.9:c.742-39_742-38delinsCT	ENSP00000367815.5:n.742-39_742-38delinsCT...
ENST00000563093.5:c.742-39_742-38delinsCT	ENSP00000457373.1:n.742-39_742-38delinsCT...
ENST00000563818.5:n.371-39_371-38delinsCT
ENST00000567666.1:n.131-39_131-38delinsCT
ENST00000567918.5:c.*61-39_*61-38delinsCT	ENSP00000455154.1:n.*61-39_*61-38delinsCT...
ENST00000570298.5:n.896-39_896-38delinsCT
NM_178452.4:c.742-39_742-38delinsCT	NP_848547.4:n.742-39_742-38delinsCT
XM_006721129.1:c.742-39_742-38delinsCT	XP_006721192.1:n.742-39_742-38delinsCT
XM_011522850.1:c.742-39_742-38delinsCT	XP_011521152.1:n.742-39_742-38delinsCT
XM_011522851.1:c.742-39_742-38delinsCT	XP_011521153.1:n.742-39_742-38delinsCT
XM_011522852.1:c.742-39_742-38delinsCT	XP_011521154.1:n.742-39_742-38delinsCT
XM_011522853.1:c.742-39_742-38delinsCT	XP_011521155.1:n.742-39_742-38delinsCT
XM_011522854.1:c.742-39_742-38delinsCT	XP_011521156.1:n.742-39_742-38delinsCT
XM_011522855.1:c.742-39_742-38delinsCT	XP_011521157.1:n.742-39_742-38delinsCT
XM_011522856.1:c.481-39_481-38delinsCT	XP_011521158.1:n.481-39_481-38delinsCT
XM_011522857.1:c.742-39_742-38delinsCT	XP_011521159.1:n.742-39_742-38delinsCT
XM_011522858.1:c.742-39_742-38delinsCT	XP_011521160.1:n.742-39_742-38delinsCT
XM_011522859.1:c.-15-39_-15-38delinsCT	XP_011521161.1:n.-15-39_-15-38delinsCT
XM_011522860.1:c.-15-39_-15-38delinsCT	XP_011521162.1:n.-15-39_-15-38delinsCT
NM_001318756.1:c.-15-39_-15-38delinsCT	NP_001305685.1:n.-15-39_-15-38delinsCT
NM_178452.5:c.742-39_742-38delinsCT	NP_848547.4:n.742-39_742-38delinsCT
XM_006721129.3:c.742-39_742-38delinsCT	XP_006721192.1:n.742-39_742-38delinsCT
XM_011522853.3:c.742-39_742-38delinsCT	XP_011521155.1:n.742-39_742-38delinsCT
XM_011522854.3:c.742-39_742-38delinsCT	XP_011521156.1:n.742-39_742-38delinsCT
XM_011522855.3:c.742-39_742-38delinsCT	XP_011521157.1:n.742-39_742-38delinsCT
XM_011522857.3:c.742-39_742-38delinsCT	XP_011521159.1:n.742-39_742-38delinsCT
XM_011522858.3:c.742-39_742-38delinsCT	XP_011521160.1:n.742-39_742-38delinsCT
XM_017022918.2:c.742-39_742-38delinsCT	XP_016878407.1:n.742-39_742-38delinsCT
XM_017022919.1:c.481-39_481-38delinsCT	XP_016878408.1:n.481-39_481-38delinsCT
XM_017022920.2:c.-15-39_-15-38delinsCT	XP_016878409.1:n.-15-39_-15-38delinsCT
XM_017022921.2:c.-15-39_-15-38delinsCT	XP_016878410.1:n.-15-39_-15-38delinsCT
XM_017022922.2:c.-15-39_-15-38delinsCT	XP_016878411.1:n.-15-39_-15-38delinsCT
XR_001751829.2:n.916-39_916-38delinsCT
XR_001751830.2:n.916-39_916-38delinsCT
XR_001751831.2:n.916-39_916-38delinsCT
XR_001751832.1:n.1225-39_1225-38delinsCT
NM_178452.6:c.742-39_742-38delinsCT MANE Select	NP_848547.4:n.742-39_742-38delinsCT