Canonical Allele Identifier: CA453966351
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21904182T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21864564T>A , CM000669.2:g.21864564T>A GRCh38
NC_000007.13:g.21904182T>A , CM000669.1:g.21904182T>A GRCh37
NC_000007.12:g.21870707T>A NCBI36
NG_012886.2:g.326350T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11403T>A MANE Select ENSP00000475939.1:p.Pro3801=
ENST00000328843.10:c.11424T>A ENSP00000330671.7:p.Pro3808=
ENST00000409508.7:c.11403T>A ENSP00000475939.1:p.Pro3801=
ENST00000620169.4:c.11424T>A ENSP00000481693.1:p.Pro3808=
NM_001277115.1:c.11403T>A NP_001264044.1:p.Pro3801=
NM_001277115.2:c.11403T>A MANE Select NP_001264044.1:p.Pro3801=
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