Canonical Allele Identifier: CA366960014
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21894006C>G (hg19) chr7:g.21854388C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21854388C>G , CM000669.2:g.21854388C>G GRCh38
NC_000007.13:g.21894006C>G , CM000669.1:g.21894006C>G GRCh37
NC_000007.12:g.21860531C>G NCBI36
NG_012886.2:g.316174C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11135C>G MANE Select ENSP00000475939.1:p.Ala3712Gly
ENST00000328843.10:c.11156C>G ENSP00000330671.7:p.Ala3719Gly
ENST00000409508.7:c.11135C>G ENSP00000475939.1:p.Ala3712Gly
ENST00000421290.1:n.318C>G
ENST00000607413.5:n.398C>G
ENST00000620169.4:c.11156C>G ENSP00000481693.1:p.Ala3719Gly
NM_001277115.1:c.11135C>G NP_001264044.1:p.Ala3712Gly
NM_001277115.2:c.11135C>G MANE Select NP_001264044.1:p.Ala3712Gly
Search 100 bp 5'
Search 100 bp 3'