Canonical Allele Identifier: CA366933396
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21635998-G-A
MyVariant Identifiers: chr7:g.21675616G>A (hg19) chr7:g.21635998G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21635998G>A , CM000669.2:g.21635998G>A GRCh38
NC_000007.13:g.21675616G>A , CM000669.1:g.21675616G>A GRCh37
NC_000007.12:g.21642141G>A NCBI36
NG_012886.2:g.97784G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4628G>A MANE Select ENSP00000475939.1:p.Trp1543Ter
ENST00000328843.10:c.4643G>A ENSP00000330671.7:p.Trp1548Ter
ENST00000409508.7:c.4628G>A ENSP00000475939.1:p.Trp1543Ter
ENST00000465593.1:n.654G>A
ENST00000620169.4:c.4643G>A ENSP00000481693.1:p.Trp1548Ter
NM_001277115.1:c.4628G>A NP_001264044.1:p.Trp1543Ter
NM_001277115.2:c.4628G>A MANE Select NP_001264044.1:p.Trp1543Ter
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