Canonical Allele Identifier: CA366944069
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21639470T>G (hg19) chr7:g.21599852T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21599852T>G , CM000669.2:g.21599852T>G GRCh38
NC_000007.13:g.21639470T>G , CM000669.1:g.21639470T>G GRCh37
NC_000007.12:g.21605995T>G NCBI36
NG_012886.2:g.61638T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.2733T>G MANE Select ENSP00000475939.1:p.Ile911Met
ENST00000328843.10:c.2733T>G ENSP00000330671.7:p.Ile911Met
ENST00000409508.7:c.2733T>G ENSP00000475939.1:p.Ile911Met
ENST00000620169.4:c.2733T>G ENSP00000481693.1:p.Ile911Met
NM_001277115.1:c.2733T>G NP_001264044.1:p.Ile911Met
NM_001277115.2:c.2733T>G MANE Select NP_001264044.1:p.Ile911Met
Search 100 bp 5'
Search 100 bp 3'