Canonical Allele Identifier: CA366955076
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21788219A>T (hg19) chr7:g.21748601A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748601A>T , CM000669.2:g.21748601A>T GRCh38
NC_000007.13:g.21788219A>T , CM000669.1:g.21788219A>T GRCh37
NC_000007.12:g.21754744A>T NCBI36
NG_012886.2:g.210387A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8532A>T MANE Select ENSP00000475939.1:p.Leu2844Phe
ENST00000328843.10:c.8553A>T ENSP00000330671.7:p.Leu2851Phe
ENST00000409508.7:c.8532A>T ENSP00000475939.1:p.Leu2844Phe
ENST00000620169.4:c.8553A>T ENSP00000481693.1:p.Leu2851Phe
NM_001277115.1:c.8532A>T NP_001264044.1:p.Leu2844Phe
NM_001277115.2:c.8532A>T MANE Select NP_001264044.1:p.Leu2844Phe
Search 100 bp 5'
Search 100 bp 3'