Canonical Allele Identifier: CA372291960

Gene: DNAAF11

Linked Data

• MyVariant Identifiers: chr8:g.133584688G>T (hg19) ; chr8:g.132572440G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572440G>T , CM000670.2:g.132572440G>T	GRCh38
NC_000008.10:g.133584688G>T , CM000670.1:g.133584688G>T	GRCh37
NC_000008.9:g.133653870G>T	NCBI36
NG_033068.1:g.108176C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1267C>A MANE Select	ENSP00000484634.1:p.His423Asn
ENST00000250173.5:c.*131C>A	ENSP00000250173.2:n.*131C>A
ENST00000518642.5:c.*131C>A	ENSP00000428610.1:n.*131C>A
ENST00000519595.5:c.1267C>A	ENSP00000429791.1:p.His423Asn
ENST00000522597.1:n.536C>A
ENST00000522789.5:c.487C>A	ENSP00000428015.1:p.His163Asn
ENST00000618342.1:c.1267C>A	ENSP00000484802.1:p.His423Asn
ENST00000620350.4:c.1267C>A	ENSP00000484634.1:p.His423Asn
NM_012472.4:c.1267C>A	NP_036604.2:p.His423Asn
NR_073525.1:n.1491C>A
XM_006716538.2:c.1285C>A	XP_006716601.2:p.His429Asn
XM_011516950.1:c.1225C>A	XP_011515252.1:p.His409Asn
XM_011516952.1:c.1021C>A	XP_011515254.1:p.His341Asn
XM_011516953.1:c.907C>A	XP_011515255.1:p.His303Asn
XM_011516954.1:c.907C>A	XP_011515256.1:p.His303Asn
XR_428377.2:n.1519C>A
NM_001321961.1:c.1207C>A	NP_001308890.1:p.His403Asn
NM_001321962.1:c.1021C>A	NP_001308891.1:p.His341Asn
NM_001321963.1:c.907C>A	NP_001308892.1:p.His303Asn
NM_001321964.1:c.907C>A	NP_001308893.1:p.His303Asn
NM_001321965.1:c.907C>A	NP_001308894.1:p.His303Asn
NM_001321966.1:c.847C>A	NP_001308895.1:p.His283Asn
NM_012472.5:c.1267C>A	NP_036604.2:p.His423Asn
NR_073525.2:n.1491C>A
NR_135905.1:n.1480C>A
NR_135906.1:n.921C>A
NR_135907.1:n.1167C>A
NR_135908.1:n.861C>A
NR_135909.1:n.1285C>A
NR_135910.1:n.1592C>A
NR_135911.1:n.1671C>A
NR_135912.1:n.2230C>A
NR_135913.1:n.1917C>A
XM_006716538.3:c.1285C>A	XP_006716601.2:p.His429Asn
XM_011516950.2:c.1225C>A	XP_011515252.1:p.His409Asn
XM_017013296.1:c.1165C>A	XP_016868785.1:p.His389Asn
XM_017013297.1:c.907C>A	XP_016868786.1:p.His303Asn
XM_017013298.1:c.907C>A	XP_016868787.1:p.His303Asn
NM_012472.6:c.1267C>A MANE Select	NP_036604.2:p.His423Asn
NM_001321961.2:c.1207C>A	NP_001308890.1:p.His403Asn
NM_001321962.2:c.1021C>A	NP_001308891.1:p.His341Asn
NM_001321963.2:c.907C>A	NP_001308892.1:p.His303Asn
NM_001321964.2:c.907C>A	NP_001308893.1:p.His303Asn
NM_001321965.2:c.907C>A	NP_001308894.1:p.His303Asn
NM_001321966.2:c.847C>A	NP_001308895.1:p.His283Asn
NR_073525.3:n.1419C>A
NR_135905.2:n.1408C>A
NR_135906.2:n.849C>A
NR_135907.2:n.1095C>A
NR_135908.2:n.789C>A
NR_135909.2:n.1305C>A
NR_135910.2:n.1655C>A
NR_135911.2:n.1775C>A
NR_135912.2:n.2334C>A
NR_135913.2:n.2021C>A