Canonical Allele Identifier: CA366955204
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21788271C>A (hg19) chr7:g.21748653C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748653C>A , CM000669.2:g.21748653C>A GRCh38
NC_000007.13:g.21788271C>A , CM000669.1:g.21788271C>A GRCh37
NC_000007.12:g.21754796C>A NCBI36
NG_012886.2:g.210439C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8584C>A MANE Select ENSP00000475939.1:p.Gln2862Lys
ENST00000328843.10:c.8605C>A ENSP00000330671.7:p.Gln2869Lys
ENST00000409508.7:c.8584C>A ENSP00000475939.1:p.Gln2862Lys
ENST00000620169.4:c.8605C>A ENSP00000481693.1:p.Gln2869Lys
NM_001277115.1:c.8584C>A NP_001264044.1:p.Gln2862Lys
NM_001277115.2:c.8584C>A MANE Select NP_001264044.1:p.Gln2862Lys
Search 100 bp 5'
Search 100 bp 3'