Canonical Allele Identifier: CA186268533

Gene: DNAAF11

Linked Data

• dbSNP Id: rs34657161
• MyVariant Identifiers: chr8:g.133584308_133584309insG (hg19) ; chr8:g.132572060_132572061insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572060_132572061insG , CM000670.2:g.132572060_132572061insG	GRCh38
NC_000008.10:g.133584308_133584309insG , CM000670.1:g.133584308_133584309insG	GRCh37
NC_000008.9:g.133653490_133653491insG	NCBI36
NG_033068.1:g.108555_108556insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.*245_*246insC MANE Select	ENSP00000484634.1:n.*245_*246insC
ENST00000618342.1:c.1646_1647insC	ENSP00000484802.1:n.1646_1647insC
ENST00000620350.4:c.*245_*246insC	ENSP00000484634.1:n.*245_*246insC
NM_012472.4:c.*245_*246insC	NP_036604.2:n.*245_*246insC
NR_073525.1:n.1870_1871insC
XM_006716538.2:c.*245_*246insC	XP_006716601.2:n.*245_*246insC
XM_011516950.1:c.*245_*246insC	XP_011515252.1:n.*245_*246insC
XM_011516952.1:c.*245_*246insC	XP_011515254.1:n.*245_*246insC
XM_011516953.1:c.*245_*246insC	XP_011515255.1:n.*245_*246insC
XM_011516954.1:c.*245_*246insC	XP_011515256.1:n.*245_*246insC
XR_428377.2:n.1898_1899insC
NM_001321961.1:c.*245_*246insC	NP_001308890.1:n.*245_*246insC
NM_001321962.1:c.*245_*246insC	NP_001308891.1:n.*245_*246insC
NM_001321963.1:c.*245_*246insC	NP_001308892.1:n.*245_*246insC
NM_001321964.1:c.*245_*246insC	NP_001308893.1:n.*245_*246insC
NM_001321965.1:c.*245_*246insC	NP_001308894.1:n.*245_*246insC
NM_001321966.1:c.*245_*246insC	NP_001308895.1:n.*245_*246insC
NM_012472.5:c.*245_*246insC	NP_036604.2:n.*245_*246insC
NR_073525.2:n.1870_1871insC
NR_135905.1:n.1859_1860insC
NR_135906.1:n.1300_1301insC
NR_135907.1:n.1546_1547insC
NR_135908.1:n.1240_1241insC
NR_135909.1:n.1664_1665insC
NR_135910.1:n.1971_1972insC
NR_135911.1:n.2050_2051insC
NR_135912.1:n.2609_2610insC
NR_135913.1:n.2296_2297insC
XM_006716538.3:c.*245_*246insC	XP_006716601.2:n.*245_*246insC
XM_011516950.2:c.*245_*246insC	XP_011515252.1:n.*245_*246insC
XM_017013296.1:c.*245_*246insC	XP_016868785.1:n.*245_*246insC
XM_017013297.1:c.*245_*246insC	XP_016868786.1:n.*245_*246insC
XM_017013298.1:c.*245_*246insC	XP_016868787.1:n.*245_*246insC
NM_012472.6:c.*245_*246insC MANE Select	NP_036604.2:n.*245_*246insC
NM_001321961.2:c.*245_*246insC	NP_001308890.1:n.*245_*246insC
NM_001321962.2:c.*245_*246insC	NP_001308891.1:n.*245_*246insC
NM_001321963.2:c.*245_*246insC	NP_001308892.1:n.*245_*246insC
NM_001321964.2:c.*245_*246insC	NP_001308893.1:n.*245_*246insC
NM_001321965.2:c.*245_*246insC	NP_001308894.1:n.*245_*246insC
NM_001321966.2:c.*245_*246insC	NP_001308895.1:n.*245_*246insC
NR_073525.3:n.1798_1799insC
NR_135905.2:n.1787_1788insC
NR_135906.2:n.1228_1229insC
NR_135907.2:n.1474_1475insC
NR_135908.2:n.1168_1169insC
NR_135909.2:n.1684_1685insC
NR_135910.2:n.2034_2035insC
NR_135911.2:n.2154_2155insC
NR_135912.2:n.2713_2714insC
NR_135913.2:n.2400_2401insC