Canonical Allele Identifier: CA1820888952
Gene: DNAAF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132661415T= , CM000670.2:g.132661415T= GRCh38
NC_000008.10:g.133673661T= , CM000670.1:g.133673661T= GRCh37
NC_000008.9:g.133742843T= NCBI36
NG_033068.1:g.19203A=

Transcript Alleles

HGVS Amino-acid change
ENST00000620350.5:c.178+45A= MANE Select ENSP00000484634.1:n.178+45A=
ENST00000250173.5:c.178+45A= ENSP00000250173.2:n.178+45A=
ENST00000518101.1:n.265+45A=
ENST00000518642.5:c.178+45A= ENSP00000428610.1:n.178+45A=
ENST00000519595.5:c.178+45A= ENSP00000429791.1:n.178+45A=
ENST00000520446.5:n.277+45A=
ENST00000521430.5:n.420+45A=
ENST00000522584.5:c.178+45A= ENSP00000429811.1:n.178+45A=
ENST00000523503.1:n.242+13903A=
ENST00000618342.1:c.178+45A= ENSP00000484802.1:n.178+45A=
ENST00000620350.4:c.178+45A= ENSP00000484634.1:n.178+45A=
NM_012472.4:c.178+45A= NP_036604.2:n.178+45A=
NR_073525.1:n.302+45A=
XM_006716538.2:c.196+45A= XP_006716601.2:n.196+45A=
XM_011516950.1:c.196+45A= XP_011515252.1:n.196+45A=
XM_011516951.1:c.196+45A= XP_011515253.1:n.196+45A=
XM_011516952.1:c.10+14069A= XP_011515254.1:n.10+14069A=
XM_011516953.1:c.-183+45A= XP_011515255.1:n.-183+45A=
XR_428377.2:n.321+45A=
NM_001321961.1:c.178+45A= NP_001308890.1:n.178+45A=
NM_001321962.1:c.10+14069A= NP_001308891.1:n.10+14069A=
NM_001321963.1:c.-183+45A= NP_001308892.1:n.-183+45A=
NM_001321964.1:c.-183+45A= NP_001308893.1:n.-183+45A=
NM_001321965.1:c.-496+45A= NP_001308894.1:n.-496+45A=
NM_001321966.1:c.-183+45A= NP_001308895.1:n.-183+45A=
NM_012472.5:c.178+45A= NP_036604.2:n.178+45A=
NR_073525.2:n.302+45A=
NR_135905.1:n.302+45A=
NR_135906.1:n.134+14069A=
NR_135907.1:n.302+45A=
NR_135908.1:n.134+14069A=
NR_135909.1:n.420+45A=
NR_135910.1:n.727+45A=
NR_135911.1:n.884+13143A=
NR_135912.1:n.1052+45A=
NR_135913.1:n.1052+45A=
XM_006716538.3:c.196+45A= XP_006716601.2:n.196+45A=
XM_011516950.2:c.196+45A= XP_011515252.1:n.196+45A=
XM_017013296.1:c.-847A= XP_016868785.1:n.-847A=
XM_017013297.1:c.-183+45A= XP_016868786.1:n.-183+45A=
XM_017013298.1:c.-287+45A= XP_016868787.1:n.-287+45A=
NM_012472.6:c.178+45A= MANE Select NP_036604.2:n.178+45A=
NM_001321961.2:c.178+45A= NP_001308890.1:n.178+45A=
NM_001321962.2:c.10+14069A= NP_001308891.1:n.10+14069A=
NM_001321963.2:c.-183+45A= NP_001308892.1:n.-183+45A=
NM_001321964.2:c.-183+45A= NP_001308893.1:n.-183+45A=
NM_001321965.2:c.-496+45A= NP_001308894.1:n.-496+45A=
NM_001321966.2:c.-183+45A= NP_001308895.1:n.-183+45A=
NR_073525.3:n.230+45A=
NR_135905.2:n.230+45A=
NR_135906.2:n.62+14069A=
NR_135907.2:n.230+45A=
NR_135908.2:n.62+14069A=
NR_135909.2:n.440+45A=
NR_135910.2:n.790+45A=
NR_135911.2:n.988+13143A=
NR_135912.2:n.1156+45A=
NR_135913.2:n.1156+45A=