Canonical Allele Identifier: CA2681976619
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21558696-A-ATGT
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21558697_21558698insGTT , CM000669.2:g.21558697_21558698insGTT GRCh38
NC_000007.13:g.21598315_21598316insGTT , CM000669.1:g.21598315_21598316insGTT GRCh37
NC_000007.12:g.21564840_21564841insGTT NCBI36
NG_012886.2:g.20483_20484insGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.496-105_496-104insGTT MANE Select ENSP00000475939.1:n.496-105_496-104insGTT
ENST00000328843.10:c.496-105_496-104insGTT ENSP00000330671.7:n.496-105_496-104insGTT
ENST00000409508.7:c.496-105_496-104insGTT ENSP00000475939.1:n.496-105_496-104insGTT
ENST00000620169.4:c.496-105_496-104insGTT ENSP00000481693.1:n.496-105_496-104insGTT
NM_001277115.1:c.496-105_496-104insGTT NP_001264044.1:n.496-105_496-104insGTT
NM_001277115.2:c.496-105_496-104insGTT MANE Select NP_001264044.1:n.496-105_496-104insGTT
Search 100 bp 5'
Search 100 bp 3'