Canonical Allele Identifier: CA155158714
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs941647236

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880786A>C , CM000669.2:g.21880786A>C GRCh38
NC_000007.13:g.21920404A>C , CM000669.1:g.21920404A>C GRCh37
NC_000007.12:g.21886929A>C NCBI36
NG_012886.2:g.342572A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12280A>C MANE Select ENSP00000475939.1:p.Arg4094=
ENST00000328843.10:c.12301A>C ENSP00000330671.7:p.Arg4101=
ENST00000409508.7:c.12280A>C ENSP00000475939.1:p.Arg4094=
ENST00000620169.4:c.12301A>C ENSP00000481693.1:p.Arg4101=
NM_001277115.1:c.12280A>C NP_001264044.1:p.Arg4094=
NM_001277115.2:c.12280A>C MANE Select NP_001264044.1:p.Arg4094=