Canonical Allele Identifier: CA847662969

Gene: DNAAF11

Linked Data

• dbSNP Id: rs1263131961
• gnomAD v3: 8-132572111-T-TAG
• gnomAD v4: 8-132572111-T-TAG
• MyVariant Identifiers: chr8:g.133584359_133584360insAG (hg19) ; chr8:g.132572111_132572112insAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572112_132572113insGA , CM000670.2:g.132572112_132572113insGA	GRCh38
NC_000008.10:g.133584360_133584361insGA , CM000670.1:g.133584360_133584361insGA	GRCh37
NC_000008.9:g.133653542_133653543insGA	NCBI36
NG_033068.1:g.108504_108505insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.*194_*195insCT MANE Select	ENSP00000484634.1:n.*194_*195insCT
ENST00000519595.5:c.*194_*195insCT	ENSP00000429791.1:n.*194_*195insCT
ENST00000618342.1:c.1595_1596insCT	ENSP00000484802.1:n.1595_1596insCT
ENST00000620350.4:c.*194_*195insCT	ENSP00000484634.1:n.*194_*195insCT
NM_012472.4:c.*194_*195insCT	NP_036604.2:n.*194_*195insCT
NR_073525.1:n.1819_1820insCT
XM_006716538.2:c.*194_*195insCT	XP_006716601.2:n.*194_*195insCT
XM_011516950.1:c.*194_*195insCT	XP_011515252.1:n.*194_*195insCT
XM_011516952.1:c.*194_*195insCT	XP_011515254.1:n.*194_*195insCT
XM_011516953.1:c.*194_*195insCT	XP_011515255.1:n.*194_*195insCT
XM_011516954.1:c.*194_*195insCT	XP_011515256.1:n.*194_*195insCT
XR_428377.2:n.1847_1848insCT
NM_001321961.1:c.*194_*195insCT	NP_001308890.1:n.*194_*195insCT
NM_001321962.1:c.*194_*195insCT	NP_001308891.1:n.*194_*195insCT
NM_001321963.1:c.*194_*195insCT	NP_001308892.1:n.*194_*195insCT
NM_001321964.1:c.*194_*195insCT	NP_001308893.1:n.*194_*195insCT
NM_001321965.1:c.*194_*195insCT	NP_001308894.1:n.*194_*195insCT
NM_001321966.1:c.*194_*195insCT	NP_001308895.1:n.*194_*195insCT
NM_012472.5:c.*194_*195insCT	NP_036604.2:n.*194_*195insCT
NR_073525.2:n.1819_1820insCT
NR_135905.1:n.1808_1809insCT
NR_135906.1:n.1249_1250insCT
NR_135907.1:n.1495_1496insCT
NR_135908.1:n.1189_1190insCT
NR_135909.1:n.1613_1614insCT
NR_135910.1:n.1920_1921insCT
NR_135911.1:n.1999_2000insCT
NR_135912.1:n.2558_2559insCT
NR_135913.1:n.2245_2246insCT
XM_006716538.3:c.*194_*195insCT	XP_006716601.2:n.*194_*195insCT
XM_011516950.2:c.*194_*195insCT	XP_011515252.1:n.*194_*195insCT
XM_017013296.1:c.*194_*195insCT	XP_016868785.1:n.*194_*195insCT
XM_017013297.1:c.*194_*195insCT	XP_016868786.1:n.*194_*195insCT
XM_017013298.1:c.*194_*195insCT	XP_016868787.1:n.*194_*195insCT
NM_012472.6:c.*194_*195insCT MANE Select	NP_036604.2:n.*194_*195insCT
NM_001321961.2:c.*194_*195insCT	NP_001308890.1:n.*194_*195insCT
NM_001321962.2:c.*194_*195insCT	NP_001308891.1:n.*194_*195insCT
NM_001321963.2:c.*194_*195insCT	NP_001308892.1:n.*194_*195insCT
NM_001321964.2:c.*194_*195insCT	NP_001308893.1:n.*194_*195insCT
NM_001321965.2:c.*194_*195insCT	NP_001308894.1:n.*194_*195insCT
NM_001321966.2:c.*194_*195insCT	NP_001308895.1:n.*194_*195insCT
NR_073525.3:n.1747_1748insCT
NR_135905.2:n.1736_1737insCT
NR_135906.2:n.1177_1178insCT
NR_135907.2:n.1423_1424insCT
NR_135908.2:n.1117_1118insCT
NR_135909.2:n.1633_1634insCT
NR_135910.2:n.1983_1984insCT
NR_135911.2:n.2103_2104insCT
NR_135912.2:n.2662_2663insCT
NR_135913.2:n.2349_2350insCT