Canonical Allele Identifier: CA1693666515
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816646G= , CM000669.2:g.21816646G= GRCh38
NC_000007.13:g.21856264G= , CM000669.1:g.21856264G= GRCh37
NC_000007.12:g.21822789G= NCBI36
NG_012886.2:g.278432G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10512G= MANE Select ENSP00000475939.1:p.Lys3504=
ENST00000328843.10:c.10533G= ENSP00000330671.7:p.Lys3511=
ENST00000409508.7:c.10512G= ENSP00000475939.1:p.Lys3504=
ENST00000620169.4:c.10533G= ENSP00000481693.1:p.Lys3511=
NM_001277115.1:c.10512G= NP_001264044.1:p.Lys3504=
NM_001277115.2:c.10512G= MANE Select NP_001264044.1:p.Lys3504=