Canonical Allele Identifier: CA453967848
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21880725-G-A
MyVariant Identifiers: chr7:g.21920343G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880725G>A , CM000669.2:g.21880725G>A GRCh38
NC_000007.13:g.21920343G>A , CM000669.1:g.21920343G>A GRCh37
NC_000007.12:g.21886868G>A NCBI36
NG_012886.2:g.342511G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12219G>A MANE Select ENSP00000475939.1:p.Lys4073=
ENST00000328843.10:c.12240G>A ENSP00000330671.7:p.Lys4080=
ENST00000409508.7:c.12219G>A ENSP00000475939.1:p.Lys4073=
ENST00000620169.4:c.12240G>A ENSP00000481693.1:p.Lys4080=
NM_001277115.1:c.12219G>A NP_001264044.1:p.Lys4073=
NM_001277115.2:c.12219G>A MANE Select NP_001264044.1:p.Lys4073=