Canonical Allele Identifier: CA366963913
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21920353T>A (hg19) chr7:g.21880735T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880735T>A , CM000669.2:g.21880735T>A GRCh38
NC_000007.13:g.21920353T>A , CM000669.1:g.21920353T>A GRCh37
NC_000007.12:g.21886878T>A NCBI36
NG_012886.2:g.342521T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.12229T>A MANE Select ENSP00000475939.1:p.Phe4077Ile
ENST00000328843.10:c.12250T>A ENSP00000330671.7:p.Phe4084Ile
ENST00000409508.7:c.12229T>A ENSP00000475939.1:p.Phe4077Ile
ENST00000620169.4:c.12250T>A ENSP00000481693.1:p.Phe4084Ile
NM_001277115.1:c.12229T>A NP_001264044.1:p.Phe4077Ile
NM_001277115.2:c.12229T>A MANE Select NP_001264044.1:p.Phe4077Ile
Search 100 bp 5'
Search 100 bp 3'