Canonical Allele Identifier: CA2527925267
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21705357-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21705357G>C , CM000669.2:g.21705357G>C GRCh38
NC_000007.13:g.21744975G>C , CM000669.1:g.21744975G>C GRCh37
NC_000007.12:g.21711500G>C NCBI36
NG_012886.2:g.167143G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.6469-103G>C MANE Select ENSP00000475939.1:n.6469-103G>C
ENST00000328843.10:c.6490-103G>C ENSP00000330671.7:n.6490-103G>C
ENST00000409508.7:c.6469-103G>C ENSP00000475939.1:n.6469-103G>C
ENST00000620169.4:c.6490-103G>C ENSP00000481693.1:n.6490-103G>C
NM_001277115.1:c.6469-103G>C NP_001264044.1:n.6469-103G>C
NM_001277115.2:c.6469-103G>C MANE Select NP_001264044.1:n.6469-103G>C