Canonical Allele Identifier: CA366964172
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21920473G>A (hg19) chr7:g.21880855G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880855G>A , CM000669.2:g.21880855G>A GRCh38
NC_000007.13:g.21920473G>A , CM000669.1:g.21920473G>A GRCh37
NC_000007.12:g.21886998G>A NCBI36
NG_012886.2:g.342641G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12349G>A MANE Select ENSP00000475939.1:p.Ala4117Thr
ENST00000328843.10:c.12370G>A ENSP00000330671.7:p.Ala4124Thr
ENST00000409508.7:c.12349G>A ENSP00000475939.1:p.Ala4117Thr
ENST00000620169.4:c.12370G>A ENSP00000481693.1:p.Ala4124Thr
NM_001277115.1:c.12349G>A NP_001264044.1:p.Ala4117Thr
NM_001277115.2:c.12349G>A MANE Select NP_001264044.1:p.Ala4117Thr
Search 100 bp 5'
Search 100 bp 3'