Canonical Allele Identifier: CA366964031
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1783893089
gnomAD v4: 7-21880787-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880787G>T , CM000669.2:g.21880787G>T GRCh38
NC_000007.13:g.21920405G>T , CM000669.1:g.21920405G>T GRCh37
NC_000007.12:g.21886930G>T NCBI36
NG_012886.2:g.342573G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12281G>T MANE Select ENSP00000475939.1:p.Arg4094Ile
ENST00000328843.10:c.12302G>T ENSP00000330671.7:p.Arg4101Ile
ENST00000409508.7:c.12281G>T ENSP00000475939.1:p.Arg4094Ile
ENST00000620169.4:c.12302G>T ENSP00000481693.1:p.Arg4101Ile
NM_001277115.1:c.12281G>T NP_001264044.1:p.Arg4094Ile
NM_001277115.2:c.12281G>T MANE Select NP_001264044.1:p.Arg4094Ile