Canonical Allele Identifier: CA2509556882
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21567600A>G , CM000669.2:g.21567600A>G GRCh38
NC_000007.13:g.21607218A>G , CM000669.1:g.21607218A>G GRCh37
NC_000007.12:g.21573743A>G NCBI36
NG_012886.2:g.29386A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.1195-2469A>G MANE Select ENSP00000475939.1:n.1195-2469A>G
ENST00000328843.10:c.1195-2469A>G ENSP00000330671.7:n.1195-2469A>G
ENST00000409508.7:c.1195-2469A>G ENSP00000475939.1:n.1195-2469A>G
ENST00000496218.1:n.81-2469A>G
ENST00000620169.4:c.1195-2469A>G ENSP00000481693.1:n.1195-2469A>G
NM_001277115.1:c.1195-2469A>G NP_001264044.1:n.1195-2469A>G
XR_927090.1:n.563+5726T>C
XR_001745114.1:n.2793+5726T>C
NM_001277115.2:c.1195-2469A>G MANE Select NP_001264044.1:n.1195-2469A>G