Canonical Allele Identifier: CA2681979370
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21599691-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21599691G>A , CM000669.2:g.21599691G>A GRCh38
NC_000007.13:g.21639309G>A , CM000669.1:g.21639309G>A GRCh37
NC_000007.12:g.21605834G>A NCBI36
NG_012886.2:g.61477G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.2668-96G>A MANE Select ENSP00000475939.1:n.2668-96G>A
ENST00000328843.10:c.2668-96G>A ENSP00000330671.7:n.2668-96G>A
ENST00000409508.7:c.2668-96G>A ENSP00000475939.1:n.2668-96G>A
ENST00000620169.4:c.2668-96G>A ENSP00000481693.1:n.2668-96G>A
NM_001277115.1:c.2668-96G>A NP_001264044.1:n.2668-96G>A
NM_001277115.2:c.2668-96G>A MANE Select NP_001264044.1:n.2668-96G>A
Search 100 bp 5'
Search 100 bp 3'