Canonical Allele Identifier: CA366955237
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1786267312
gnomAD v4: 7-21748661-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748661G>C , CM000669.2:g.21748661G>C GRCh38
NC_000007.13:g.21788279G>C , CM000669.1:g.21788279G>C GRCh37
NC_000007.12:g.21754804G>C NCBI36
NG_012886.2:g.210447G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8592G>C MANE Select ENSP00000475939.1:p.Leu2864Phe
ENST00000328843.10:c.8613G>C ENSP00000330671.7:p.Leu2871Phe
ENST00000409508.7:c.8592G>C ENSP00000475939.1:p.Leu2864Phe
ENST00000620169.4:c.8613G>C ENSP00000481693.1:p.Leu2871Phe
NM_001277115.1:c.8592G>C NP_001264044.1:p.Leu2864Phe
NM_001277115.2:c.8592G>C MANE Select NP_001264044.1:p.Leu2864Phe