Canonical Allele Identifier: CA4881486

Gene: DNAAF11

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132661606C>T , CM000670.2:g.132661606C>T	GRCh38
NC_000008.10:g.133673852C>T , CM000670.1:g.133673852C>T	GRCh37
NC_000008.9:g.133743034C>T	NCBI36
NG_033068.1:g.19012G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012472.6:c.32G>A MANE Select	NP_036604.2:p.Arg11Gln
ENST00000620350.5:c.32G>A MANE Select	ENSP00000484634.1:p.Arg11Gln
NM_001321961.1:c.32G>A	NP_001308890.1:p.Arg11Gln
NM_001321961.2:c.32G>A	NP_001308890.1:p.Arg11Gln
NM_001321962.1:c.10+13878G>A	NP_001308891.1:n.10+13878G>A
NM_001321962.2:c.10+13878G>A	NP_001308891.1:n.10+13878G>A
NM_001321963.1:c.-329G>A	NP_001308892.1:n.-329G>A
NM_001321963.2:c.-329G>A	NP_001308892.1:n.-329G>A
NM_001321964.1:c.-329G>A	NP_001308893.1:n.-329G>A
NM_001321964.2:c.-329G>A	NP_001308893.1:n.-329G>A
NM_001321965.1:c.-642G>A	NP_001308894.1:n.-642G>A
NM_001321965.2:c.-642G>A	NP_001308894.1:n.-642G>A
NM_001321966.1:c.-329G>A	NP_001308895.1:n.-329G>A
NM_001321966.2:c.-329G>A	NP_001308895.1:n.-329G>A
NM_012472.4:c.32G>A	NP_036604.2:p.Arg11Gln
NM_012472.5:c.32G>A	NP_036604.2:p.Arg11Gln
NR_073525.1:n.156G>A
NR_073525.2:n.156G>A
NR_073525.3:n.84G>A
NR_135905.1:n.156G>A
NR_135905.2:n.84G>A
NR_135906.1:n.134+13878G>A
NR_135906.2:n.62+13878G>A
NR_135907.1:n.156G>A
NR_135907.2:n.84G>A
NR_135908.1:n.134+13878G>A
NR_135908.2:n.62+13878G>A
NR_135909.1:n.274G>A
NR_135909.2:n.294G>A
NR_135910.1:n.581G>A
NR_135910.2:n.644G>A
NR_135911.1:n.884+12952G>A
NR_135911.2:n.988+12952G>A
NR_135912.1:n.906G>A
NR_135912.2:n.1010G>A
NR_135913.1:n.906G>A
NR_135913.2:n.1010G>A
ENST00000250173.5:c.32G>A	ENSP00000250173.2:p.Arg11Gln
ENST00000518101.1:n.119G>A
ENST00000518642.5:c.32G>A	ENSP00000428610.1:p.Arg11Gln
ENST00000519595.5:c.32G>A	ENSP00000429791.1:p.Arg11Gln
ENST00000520446.5:n.131G>A
ENST00000521430.5:n.274G>A
ENST00000522584.5:c.32G>A	ENSP00000429811.1:p.Arg11Gln
ENST00000523503.1:n.242+13712G>A
ENST00000618342.1:c.32G>A	ENSP00000484802.1:p.Arg11Gln
ENST00000620350.4:c.32G>A	ENSP00000484634.1:p.Arg11Gln
XM_006716538.2:c.50G>A	XP_006716601.2:p.Arg17Gln
XM_006716538.3:c.50G>A	XP_006716601.2:p.Arg17Gln
XM_011516950.1:c.50G>A	XP_011515252.1:p.Arg17Gln
XM_011516950.2:c.50G>A	XP_011515252.1:p.Arg17Gln
XM_011516951.1:c.50G>A	XP_011515253.1:p.Arg17Gln
XM_011516952.1:c.10+13878G>A	XP_011515254.1:n.10+13878G>A
XM_011516953.1:c.-329G>A	XP_011515255.1:n.-329G>A
XM_017013297.1:c.-329G>A	XP_016868786.1:n.-329G>A
XM_017013298.1:c.-433G>A	XP_016868787.1:n.-433G>A
XR_428377.2:n.175G>A