Canonical Allele Identifier: CA186274935

Gene: DNAAF11

Linked Data

• dbSNP Id: rs1037263244
• gnomAD v3: 8-132632979-T-C
• gnomAD v4: 8-132632979-T-C
• MyVariant Identifiers: chr8:g.133645225T>C (hg19) ; chr8:g.132632979T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132632979T>C , CM000670.2:g.132632979T>C	GRCh38
NC_000008.10:g.133645225T>C , CM000670.1:g.133645225T>C	GRCh37
NC_000008.9:g.133714407T>C	NCBI36
NG_033068.1:g.47639A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000620350.5:c.430-16A>G MANE Select	ENSP00000484634.1:n.430-16A>G
ENST00000250173.5:c.430-16A>G	ENSP00000250173.2:n.430-16A>G
ENST00000518642.5:c.430-16A>G	ENSP00000428610.1:n.430-16A>G
ENST00000519595.5:c.430-16A>G	ENSP00000429791.1:n.430-16A>G
ENST00000520446.5:n.528+4956A>G
ENST00000523503.1:n.415+4956A>G
ENST00000618342.1:c.430-16A>G	ENSP00000484802.1:n.430-16A>G
ENST00000620350.4:c.430-16A>G	ENSP00000484634.1:n.430-16A>G
NM_012472.4:c.430-16A>G	NP_036604.2:n.430-16A>G
NR_073525.1:n.554-16A>G
XM_006716538.2:c.448-16A>G	XP_006716601.2:n.448-16A>G
XM_011516950.1:c.448-16A>G	XP_011515252.1:n.448-16A>G
XM_011516951.1:c.448-16A>G	XP_011515253.1:n.448-16A>G
XM_011516952.1:c.184-16A>G	XP_011515254.1:n.184-16A>G
XM_011516953.1:c.70-16A>G	XP_011515255.1:n.70-16A>G
XM_011516954.1:c.70-16A>G	XP_011515256.1:n.70-16A>G
XR_428377.2:n.573-16A>G
NM_001321961.1:c.430-16A>G	NP_001308890.1:n.430-16A>G
NM_001321962.1:c.184-16A>G	NP_001308891.1:n.184-16A>G
NM_001321963.1:c.70-16A>G	NP_001308892.1:n.70-16A>G
NM_001321964.1:c.70-16A>G	NP_001308893.1:n.70-16A>G
NM_001321965.1:c.70-16A>G	NP_001308894.1:n.70-16A>G
NM_001321966.1:c.70-16A>G	NP_001308895.1:n.70-16A>G
NM_012472.5:c.430-16A>G	NP_036604.2:n.430-16A>G
NR_073525.2:n.554-16A>G
NR_135905.1:n.866+4956A>G
NR_135906.1:n.307+4956A>G
NR_135907.1:n.553+4956A>G
NR_135908.1:n.307+4956A>G
NR_135909.1:n.671+4956A>G
NR_135910.1:n.978+4956A>G
NR_135911.1:n.1057+4956A>G
NR_135912.1:n.1616+4956A>G
NR_135913.1:n.1303+4956A>G
XM_006716538.3:c.448-16A>G	XP_006716601.2:n.448-16A>G
XM_011516950.2:c.448-16A>G	XP_011515252.1:n.448-16A>G
XM_017013296.1:c.328-16A>G	XP_016868785.1:n.328-16A>G
XM_017013297.1:c.70-16A>G	XP_016868786.1:n.70-16A>G
XM_017013298.1:c.70-16A>G	XP_016868787.1:n.70-16A>G
NM_012472.6:c.430-16A>G MANE Select	NP_036604.2:n.430-16A>G
NM_001321961.2:c.430-16A>G	NP_001308890.1:n.430-16A>G
NM_001321962.2:c.184-16A>G	NP_001308891.1:n.184-16A>G
NM_001321963.2:c.70-16A>G	NP_001308892.1:n.70-16A>G
NM_001321964.2:c.70-16A>G	NP_001308893.1:n.70-16A>G
NM_001321965.2:c.70-16A>G	NP_001308894.1:n.70-16A>G
NM_001321966.2:c.70-16A>G	NP_001308895.1:n.70-16A>G
NR_073525.3:n.482-16A>G
NR_135905.2:n.794+4956A>G
NR_135906.2:n.235+4956A>G
NR_135907.2:n.481+4956A>G
NR_135908.2:n.235+4956A>G
NR_135909.2:n.691+4956A>G
NR_135910.2:n.1041+4956A>G
NR_135911.2:n.1161+4956A>G
NR_135912.2:n.1720+4956A>G
NR_135913.2:n.1407+4956A>G