Canonical Allele Identifier: CA2511744272
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21558699_21558700insGAAG , CM000669.2:g.21558699_21558700insGAAG GRCh38
NC_000007.13:g.21598317_21598318insGAAG , CM000669.1:g.21598317_21598318insGAAG GRCh37
NC_000007.12:g.21564842_21564843insGAAG NCBI36
NG_012886.2:g.20485_20486insGAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.496-103_496-102insGAAG MANE Select ENSP00000475939.1:n.496-103_496-102insGAAG
ENST00000328843.10:c.496-103_496-102insGAAG ENSP00000330671.7:n.496-103_496-102insGAAG
ENST00000409508.7:c.496-103_496-102insGAAG ENSP00000475939.1:n.496-103_496-102insGAAG
ENST00000620169.4:c.496-103_496-102insGAAG ENSP00000481693.1:n.496-103_496-102insGAAG
NM_001277115.1:c.496-103_496-102insGAAG NP_001264044.1:n.496-103_496-102insGAAG
NM_001277115.2:c.496-103_496-102insGAAG MANE Select NP_001264044.1:n.496-103_496-102insGAAG