Canonical Allele Identifier: CA1693557641
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21567705T= , CM000669.2:g.21567705T= GRCh38
NC_000007.13:g.21607323T= , CM000669.1:g.21607323T= GRCh37
NC_000007.12:g.21573848T= NCBI36
NG_012886.2:g.29491T=

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.1195-2364T= MANE Select ENSP00000475939.1:n.1195-2364T=
ENST00000328843.10:c.1195-2364T= ENSP00000330671.7:n.1195-2364T=
ENST00000409508.7:c.1195-2364T= ENSP00000475939.1:n.1195-2364T=
ENST00000496218.1:n.81-2364T=
ENST00000620169.4:c.1195-2364T= ENSP00000481693.1:n.1195-2364T=
NM_001277115.1:c.1195-2364T= NP_001264044.1:n.1195-2364T=
XR_927090.1:n.563+5621A=
XR_001745114.1:n.2793+5621A=
NM_001277115.2:c.1195-2364T= MANE Select NP_001264044.1:n.1195-2364T=
Search 100 bp 5'
Search 100 bp 3'