Canonical Allele Identifier: CA372291918

Gene: DNAAF11

Linked Data

• MyVariant Identifiers: chr8:g.133584670T>A (hg19) ; chr8:g.132572422T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572422T>A , CM000670.2:g.132572422T>A	GRCh38
NC_000008.10:g.133584670T>A , CM000670.1:g.133584670T>A	GRCh37
NC_000008.9:g.133653852T>A	NCBI36
NG_033068.1:g.108194A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1285A>T MANE Select	ENSP00000484634.1:p.Thr429Ser
ENST00000250173.5:c.*149A>T	ENSP00000250173.2:n.*149A>T
ENST00000518642.5:c.*149A>T	ENSP00000428610.1:n.*149A>T
ENST00000519595.5:c.1285A>T	ENSP00000429791.1:p.Thr429Ser
ENST00000522789.5:c.505A>T	ENSP00000428015.1:p.Thr169Ser
ENST00000618342.1:c.1285A>T	ENSP00000484802.1:p.Thr429Ser
ENST00000620350.4:c.1285A>T	ENSP00000484634.1:p.Thr429Ser
NM_012472.4:c.1285A>T	NP_036604.2:p.Thr429Ser
NR_073525.1:n.1509A>T
XM_006716538.2:c.1303A>T	XP_006716601.2:p.Thr435Ser
XM_011516950.1:c.1243A>T	XP_011515252.1:p.Thr415Ser
XM_011516952.1:c.1039A>T	XP_011515254.1:p.Thr347Ser
XM_011516953.1:c.925A>T	XP_011515255.1:p.Thr309Ser
XM_011516954.1:c.925A>T	XP_011515256.1:p.Thr309Ser
XR_428377.2:n.1537A>T
NM_001321961.1:c.1225A>T	NP_001308890.1:p.Thr409Ser
NM_001321962.1:c.1039A>T	NP_001308891.1:p.Thr347Ser
NM_001321963.1:c.925A>T	NP_001308892.1:p.Thr309Ser
NM_001321964.1:c.925A>T	NP_001308893.1:p.Thr309Ser
NM_001321965.1:c.925A>T	NP_001308894.1:p.Thr309Ser
NM_001321966.1:c.865A>T	NP_001308895.1:p.Thr289Ser
NM_012472.5:c.1285A>T	NP_036604.2:p.Thr429Ser
NR_073525.2:n.1509A>T
NR_135905.1:n.1498A>T
NR_135906.1:n.939A>T
NR_135907.1:n.1185A>T
NR_135908.1:n.879A>T
NR_135909.1:n.1303A>T
NR_135910.1:n.1610A>T
NR_135911.1:n.1689A>T
NR_135912.1:n.2248A>T
NR_135913.1:n.1935A>T
XM_006716538.3:c.1303A>T	XP_006716601.2:p.Thr435Ser
XM_011516950.2:c.1243A>T	XP_011515252.1:p.Thr415Ser
XM_017013296.1:c.1183A>T	XP_016868785.1:p.Thr395Ser
XM_017013297.1:c.925A>T	XP_016868786.1:p.Thr309Ser
XM_017013298.1:c.925A>T	XP_016868787.1:p.Thr309Ser
NM_012472.6:c.1285A>T MANE Select	NP_036604.2:p.Thr429Ser
NM_001321961.2:c.1225A>T	NP_001308890.1:p.Thr409Ser
NM_001321962.2:c.1039A>T	NP_001308891.1:p.Thr347Ser
NM_001321963.2:c.925A>T	NP_001308892.1:p.Thr309Ser
NM_001321964.2:c.925A>T	NP_001308893.1:p.Thr309Ser
NM_001321965.2:c.925A>T	NP_001308894.1:p.Thr309Ser
NM_001321966.2:c.865A>T	NP_001308895.1:p.Thr289Ser
NR_073525.3:n.1437A>T
NR_135905.2:n.1426A>T
NR_135906.2:n.867A>T
NR_135907.2:n.1113A>T
NR_135908.2:n.807A>T
NR_135909.2:n.1323A>T
NR_135910.2:n.1673A>T
NR_135911.2:n.1793A>T
NR_135912.2:n.2352A>T
NR_135913.2:n.2039A>T