Canonical Allele Identifier: CA652762969

Gene: DNAAF11

Linked Data

• gnomAD v4: 8-132572077-A-T
• COSMIC: COSN15704180

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572077A>T , CM000670.2:g.132572077A>T	GRCh38
NC_000008.10:g.133584325A>T , CM000670.1:g.133584325A>T	GRCh37
NC_000008.9:g.133653507A>T	NCBI36
NG_033068.1:g.108539T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.*229T>A MANE Select	ENSP00000484634.1:n.*229T>A
ENST00000519595.5:c.*229T>A	ENSP00000429791.1:n.*229T>A
ENST00000618342.1:c.1630T>A	ENSP00000484802.1:n.1630T>A
ENST00000620350.4:c.*229T>A	ENSP00000484634.1:n.*229T>A
NM_012472.4:c.*229T>A	NP_036604.2:n.*229T>A
NR_073525.1:n.1854T>A
XM_006716538.2:c.*229T>A	XP_006716601.2:n.*229T>A
XM_011516950.1:c.*229T>A	XP_011515252.1:n.*229T>A
XM_011516952.1:c.*229T>A	XP_011515254.1:n.*229T>A
XM_011516953.1:c.*229T>A	XP_011515255.1:n.*229T>A
XM_011516954.1:c.*229T>A	XP_011515256.1:n.*229T>A
XR_428377.2:n.1882T>A
NM_001321961.1:c.*229T>A	NP_001308890.1:n.*229T>A
NM_001321962.1:c.*229T>A	NP_001308891.1:n.*229T>A
NM_001321963.1:c.*229T>A	NP_001308892.1:n.*229T>A
NM_001321964.1:c.*229T>A	NP_001308893.1:n.*229T>A
NM_001321965.1:c.*229T>A	NP_001308894.1:n.*229T>A
NM_001321966.1:c.*229T>A	NP_001308895.1:n.*229T>A
NM_012472.5:c.*229T>A	NP_036604.2:n.*229T>A
NR_073525.2:n.1854T>A
NR_135905.1:n.1843T>A
NR_135906.1:n.1284T>A
NR_135907.1:n.1530T>A
NR_135908.1:n.1224T>A
NR_135909.1:n.1648T>A
NR_135910.1:n.1955T>A
NR_135911.1:n.2034T>A
NR_135912.1:n.2593T>A
NR_135913.1:n.2280T>A
XM_006716538.3:c.*229T>A	XP_006716601.2:n.*229T>A
XM_011516950.2:c.*229T>A	XP_011515252.1:n.*229T>A
XM_017013296.1:c.*229T>A	XP_016868785.1:n.*229T>A
XM_017013297.1:c.*229T>A	XP_016868786.1:n.*229T>A
XM_017013298.1:c.*229T>A	XP_016868787.1:n.*229T>A
NM_012472.6:c.*229T>A MANE Select	NP_036604.2:n.*229T>A
NM_001321961.2:c.*229T>A	NP_001308890.1:n.*229T>A
NM_001321962.2:c.*229T>A	NP_001308891.1:n.*229T>A
NM_001321963.2:c.*229T>A	NP_001308892.1:n.*229T>A
NM_001321964.2:c.*229T>A	NP_001308893.1:n.*229T>A
NM_001321965.2:c.*229T>A	NP_001308894.1:n.*229T>A
NM_001321966.2:c.*229T>A	NP_001308895.1:n.*229T>A
NR_073525.3:n.1782T>A
NR_135905.2:n.1771T>A
NR_135906.2:n.1212T>A
NR_135907.2:n.1458T>A
NR_135908.2:n.1152T>A
NR_135909.2:n.1668T>A
NR_135910.2:n.2018T>A
NR_135911.2:n.2138T>A
NR_135912.2:n.2697T>A
NR_135913.2:n.2384T>A