Canonical Allele Identifier: CA366963977
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21880763-A-T
MyVariant Identifiers: chr7:g.21920381A>T (hg19) chr7:g.21880763A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880763A>T , CM000669.2:g.21880763A>T GRCh38
NC_000007.13:g.21920381A>T , CM000669.1:g.21920381A>T GRCh37
NC_000007.12:g.21886906A>T NCBI36
NG_012886.2:g.342549A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12257A>T MANE Select ENSP00000475939.1:p.Tyr4086Phe
ENST00000328843.10:c.12278A>T ENSP00000330671.7:p.Tyr4093Phe
ENST00000409508.7:c.12257A>T ENSP00000475939.1:p.Tyr4086Phe
ENST00000620169.4:c.12278A>T ENSP00000481693.1:p.Tyr4093Phe
NM_001277115.1:c.12257A>T NP_001264044.1:p.Tyr4086Phe
NM_001277115.2:c.12257A>T MANE Select NP_001264044.1:p.Tyr4086Phe
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