Canonical Allele Identifier: CA366933629
Gene: DNAH11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21636056A>T , CM000669.2:g.21636056A>T GRCh38
NC_000007.13:g.21675674A>T , CM000669.1:g.21675674A>T GRCh37
NC_000007.12:g.21642199A>T NCBI36
NG_012886.2:g.97842A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4686A>T MANE Select ENSP00000475939.1:p.Lys1562Asn
ENST00000328843.10:c.4701A>T ENSP00000330671.7:p.Lys1567Asn
ENST00000409508.7:c.4686A>T ENSP00000475939.1:p.Lys1562Asn
ENST00000465593.1:n.712A>T
ENST00000620169.4:c.4701A>T ENSP00000481693.1:p.Lys1567Asn
NM_001277115.1:c.4686A>T NP_001264044.1:p.Lys1562Asn
NM_001277115.2:c.4686A>T MANE Select NP_001264044.1:p.Lys1562Asn