Canonical Allele Identifier: CA2238462053

Gene: DNAAF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84159737C= , CM000678.2:g.84159737C=	GRCh38
NC_000016.9:g.84193342C= , CM000678.1:g.84193342C=	GRCh37
NC_000016.8:g.82750843C=	NCBI36
NG_021174.1:g.19478C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378553.10:c.804C= MANE Select	ENSP00000367815.5:p.Val268=
ENST00000378553.9:c.804C=	ENSP00000367815.5:p.Val268=
ENST00000563093.5:c.804C=	ENSP00000457373.1:p.Val268=
ENST00000563818.5:n.433C=
ENST00000567666.1:n.193C=
ENST00000567918.5:c.*123C=	ENSP00000455154.1:n.*123C=
ENST00000570298.5:n.958C=
NM_178452.4:c.804C=	NP_848547.4:p.Val268=
XM_006721129.1:c.804C=	XP_006721192.1:p.Val268=
XM_011522850.1:c.804C=	XP_011521152.1:p.Val268=
XM_011522851.1:c.804C=	XP_011521153.1:p.Val268=
XM_011522852.1:c.804C=	XP_011521154.1:p.Val268=
XM_011522853.1:c.804C=	XP_011521155.1:p.Val268=
XM_011522854.1:c.804C=	XP_011521156.1:p.Val268=
XM_011522855.1:c.804C=	XP_011521157.1:p.Val268=
XM_011522856.1:c.543C=	XP_011521158.1:p.Val181=
XM_011522857.1:c.804C=	XP_011521159.1:p.Val268=
XM_011522858.1:c.804C=	XP_011521160.1:p.Val268=
XM_011522859.1:c.48C=	XP_011521161.1:p.Val16=
XM_011522860.1:c.48C=	XP_011521162.1:p.Val16=
NM_001318756.1:c.48C=	NP_001305685.1:p.Val16=
NM_178452.5:c.804C=	NP_848547.4:p.Val268=
XM_006721129.3:c.804C=	XP_006721192.1:p.Val268=
XM_011522853.3:c.804C=	XP_011521155.1:p.Val268=
XM_011522854.3:c.804C=	XP_011521156.1:p.Val268=
XM_011522855.3:c.804C=	XP_011521157.1:p.Val268=
XM_011522857.3:c.804C=	XP_011521159.1:p.Val268=
XM_011522858.3:c.804C=	XP_011521160.1:p.Val268=
XM_017022918.2:c.804C=	XP_016878407.1:p.Val268=
XM_017022919.1:c.543C=	XP_016878408.1:p.Val181=
XM_017022920.2:c.48C=	XP_016878409.1:p.Val16=
XM_017022921.2:c.48C=	XP_016878410.1:p.Val16=
XM_017022922.2:c.48C=	XP_016878411.1:p.Val16=
XR_001751829.2:n.978C=
XR_001751830.2:n.978C=
XR_001751831.2:n.978C=
XR_001751832.1:n.1287C=
NM_178452.6:c.804C= MANE Select	NP_848547.4:p.Val268=