Canonical Allele Identifier: CA372291924

Gene: DNAAF11

Linked Data

• MyVariant Identifiers: chr8:g.133584673C>A (hg19) ; chr8:g.132572425C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572425C>A , CM000670.2:g.132572425C>A	GRCh38
NC_000008.10:g.133584673C>A , CM000670.1:g.133584673C>A	GRCh37
NC_000008.9:g.133653855C>A	NCBI36
NG_033068.1:g.108191G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1282G>T MANE Select	ENSP00000484634.1:p.Val428Leu
ENST00000250173.5:c.*146G>T	ENSP00000250173.2:n.*146G>T
ENST00000518642.5:c.*146G>T	ENSP00000428610.1:n.*146G>T
ENST00000519595.5:c.1282G>T	ENSP00000429791.1:p.Val428Leu
ENST00000522597.1:n.551G>T
ENST00000522789.5:c.502G>T	ENSP00000428015.1:p.Val168Leu
ENST00000618342.1:c.1282G>T	ENSP00000484802.1:p.Val428Leu
ENST00000620350.4:c.1282G>T	ENSP00000484634.1:p.Val428Leu
NM_012472.4:c.1282G>T	NP_036604.2:p.Val428Leu
NR_073525.1:n.1506G>T
XM_006716538.2:c.1300G>T	XP_006716601.2:p.Val434Leu
XM_011516950.1:c.1240G>T	XP_011515252.1:p.Val414Leu
XM_011516952.1:c.1036G>T	XP_011515254.1:p.Val346Leu
XM_011516953.1:c.922G>T	XP_011515255.1:p.Val308Leu
XM_011516954.1:c.922G>T	XP_011515256.1:p.Val308Leu
XR_428377.2:n.1534G>T
NM_001321961.1:c.1222G>T	NP_001308890.1:p.Val408Leu
NM_001321962.1:c.1036G>T	NP_001308891.1:p.Val346Leu
NM_001321963.1:c.922G>T	NP_001308892.1:p.Val308Leu
NM_001321964.1:c.922G>T	NP_001308893.1:p.Val308Leu
NM_001321965.1:c.922G>T	NP_001308894.1:p.Val308Leu
NM_001321966.1:c.862G>T	NP_001308895.1:p.Val288Leu
NM_012472.5:c.1282G>T	NP_036604.2:p.Val428Leu
NR_073525.2:n.1506G>T
NR_135905.1:n.1495G>T
NR_135906.1:n.936G>T
NR_135907.1:n.1182G>T
NR_135908.1:n.876G>T
NR_135909.1:n.1300G>T
NR_135910.1:n.1607G>T
NR_135911.1:n.1686G>T
NR_135912.1:n.2245G>T
NR_135913.1:n.1932G>T
XM_006716538.3:c.1300G>T	XP_006716601.2:p.Val434Leu
XM_011516950.2:c.1240G>T	XP_011515252.1:p.Val414Leu
XM_017013296.1:c.1180G>T	XP_016868785.1:p.Val394Leu
XM_017013297.1:c.922G>T	XP_016868786.1:p.Val308Leu
XM_017013298.1:c.922G>T	XP_016868787.1:p.Val308Leu
NM_012472.6:c.1282G>T MANE Select	NP_036604.2:p.Val428Leu
NM_001321961.2:c.1222G>T	NP_001308890.1:p.Val408Leu
NM_001321962.2:c.1036G>T	NP_001308891.1:p.Val346Leu
NM_001321963.2:c.922G>T	NP_001308892.1:p.Val308Leu
NM_001321964.2:c.922G>T	NP_001308893.1:p.Val308Leu
NM_001321965.2:c.922G>T	NP_001308894.1:p.Val308Leu
NM_001321966.2:c.862G>T	NP_001308895.1:p.Val288Leu
NR_073525.3:n.1434G>T
NR_135905.2:n.1423G>T
NR_135906.2:n.864G>T
NR_135907.2:n.1110G>T
NR_135908.2:n.804G>T
NR_135909.2:n.1320G>T
NR_135910.2:n.1670G>T
NR_135911.2:n.1790G>T
NR_135912.2:n.2349G>T
NR_135913.2:n.2036G>T