Canonical Allele Identifier: CA366949167
Gene: DNAH11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816678A>C , CM000669.2:g.21816678A>C GRCh38
NC_000007.13:g.21856296A>C , CM000669.1:g.21856296A>C GRCh37
NC_000007.12:g.21822821A>C NCBI36
NG_012886.2:g.278464A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10544A>C MANE Select ENSP00000475939.1:p.Lys3515Thr
ENST00000328843.10:c.10565A>C ENSP00000330671.7:p.Lys3522Thr
ENST00000409508.7:c.10544A>C ENSP00000475939.1:p.Lys3515Thr
ENST00000620169.4:c.10565A>C ENSP00000481693.1:p.Lys3522Thr
NM_001277115.1:c.10544A>C NP_001264044.1:p.Lys3515Thr
NM_001277115.2:c.10544A>C MANE Select NP_001264044.1:p.Lys3515Thr