Canonical Allele Identifier: CA1693538824
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1783315795

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21558633_21558634insGTTGATTA , CM000669.2:g.21558633_21558634insGTTGATTA GRCh38
NC_000007.13:g.21598251_21598252insGTTGATTA , CM000669.1:g.21598251_21598252insGTTGATTA GRCh37
NC_000007.12:g.21564776_21564777insGTTGATTA NCBI36
NG_012886.2:g.20419_20420insGTTGATTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.496-169_496-168insGTTGATTA MANE Select ENSP00000475939.1:n.496-169_496-168insGTTGATTA
ENST00000328843.10:c.496-169_496-168insGTTGATTA ENSP00000330671.7:n.496-169_496-168insGTTGATTA
ENST00000409508.7:c.496-169_496-168insGTTGATTA ENSP00000475939.1:n.496-169_496-168insGTTGATTA
ENST00000620169.4:c.496-169_496-168insGTTGATTA ENSP00000481693.1:n.496-169_496-168insGTTGATTA
NM_001277115.1:c.496-169_496-168insGTTGATTA NP_001264044.1:n.496-169_496-168insGTTGATTA
NM_001277115.2:c.496-169_496-168insGTTGATTA MANE Select NP_001264044.1:n.496-169_496-168insGTTGATTA