Canonical Allele Identifier: CA372291745

Gene: DNAAF11

Linked Data

• MyVariant Identifiers: chr8:g.133584588A>T (hg19) ; chr8:g.132572340A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572340A>T , CM000670.2:g.132572340A>T	GRCh38
NC_000008.10:g.133584588A>T , CM000670.1:g.133584588A>T	GRCh37
NC_000008.9:g.133653770A>T	NCBI36
NG_033068.1:g.108276T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1367T>A MANE Select	ENSP00000484634.1:p.Phe456Tyr
ENST00000250173.5:c.*231T>A	ENSP00000250173.2:n.*231T>A
ENST00000518642.5:c.*231T>A	ENSP00000428610.1:n.*231T>A
ENST00000519595.5:c.1367T>A	ENSP00000429791.1:p.Phe456Tyr
ENST00000522789.5:c.587T>A	ENSP00000428015.1:p.Phe196Tyr
ENST00000618342.1:c.1367T>A	ENSP00000484802.1:p.Phe456Tyr
ENST00000620350.4:c.1367T>A	ENSP00000484634.1:p.Phe456Tyr
NM_012472.4:c.1367T>A	NP_036604.2:p.Phe456Tyr
NR_073525.1:n.1591T>A
XM_006716538.2:c.1385T>A	XP_006716601.2:p.Phe462Tyr
XM_011516950.1:c.1325T>A	XP_011515252.1:p.Phe442Tyr
XM_011516952.1:c.1121T>A	XP_011515254.1:p.Phe374Tyr
XM_011516953.1:c.1007T>A	XP_011515255.1:p.Phe336Tyr
XM_011516954.1:c.1007T>A	XP_011515256.1:p.Phe336Tyr
XR_428377.2:n.1619T>A
NM_001321961.1:c.1307T>A	NP_001308890.1:p.Phe436Tyr
NM_001321962.1:c.1121T>A	NP_001308891.1:p.Phe374Tyr
NM_001321963.1:c.1007T>A	NP_001308892.1:p.Phe336Tyr
NM_001321964.1:c.1007T>A	NP_001308893.1:p.Phe336Tyr
NM_001321965.1:c.1007T>A	NP_001308894.1:p.Phe336Tyr
NM_001321966.1:c.947T>A	NP_001308895.1:p.Phe316Tyr
NM_012472.5:c.1367T>A	NP_036604.2:p.Phe456Tyr
NR_073525.2:n.1591T>A
NR_135905.1:n.1580T>A
NR_135906.1:n.1021T>A
NR_135907.1:n.1267T>A
NR_135908.1:n.961T>A
NR_135909.1:n.1385T>A
NR_135910.1:n.1692T>A
NR_135911.1:n.1771T>A
NR_135912.1:n.2330T>A
NR_135913.1:n.2017T>A
XM_006716538.3:c.1385T>A	XP_006716601.2:p.Phe462Tyr
XM_011516950.2:c.1325T>A	XP_011515252.1:p.Phe442Tyr
XM_017013296.1:c.1265T>A	XP_016868785.1:p.Phe422Tyr
XM_017013297.1:c.1007T>A	XP_016868786.1:p.Phe336Tyr
XM_017013298.1:c.1007T>A	XP_016868787.1:p.Phe336Tyr
NM_012472.6:c.1367T>A MANE Select	NP_036604.2:p.Phe456Tyr
NM_001321961.2:c.1307T>A	NP_001308890.1:p.Phe436Tyr
NM_001321962.2:c.1121T>A	NP_001308891.1:p.Phe374Tyr
NM_001321963.2:c.1007T>A	NP_001308892.1:p.Phe336Tyr
NM_001321964.2:c.1007T>A	NP_001308893.1:p.Phe336Tyr
NM_001321965.2:c.1007T>A	NP_001308894.1:p.Phe336Tyr
NM_001321966.2:c.947T>A	NP_001308895.1:p.Phe316Tyr
NR_073525.3:n.1519T>A
NR_135905.2:n.1508T>A
NR_135906.2:n.949T>A
NR_135907.2:n.1195T>A
NR_135908.2:n.889T>A
NR_135909.2:n.1405T>A
NR_135910.2:n.1755T>A
NR_135911.2:n.1875T>A
NR_135912.2:n.2434T>A
NR_135913.2:n.2121T>A