Canonical Allele Identifier: CA366959978
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21893997C>G (hg19) chr7:g.21854379C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21854379C>G , CM000669.2:g.21854379C>G GRCh38
NC_000007.13:g.21893997C>G , CM000669.1:g.21893997C>G GRCh37
NC_000007.12:g.21860522C>G NCBI36
NG_012886.2:g.316165C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11126C>G MANE Select ENSP00000475939.1:p.Ala3709Gly
ENST00000328843.10:c.11147C>G ENSP00000330671.7:p.Ala3716Gly
ENST00000409508.7:c.11126C>G ENSP00000475939.1:p.Ala3709Gly
ENST00000421290.1:n.309C>G
ENST00000607413.5:n.389C>G
ENST00000620169.4:c.11147C>G ENSP00000481693.1:p.Ala3716Gly
NM_001277115.1:c.11126C>G NP_001264044.1:p.Ala3709Gly
NM_001277115.2:c.11126C>G MANE Select NP_001264044.1:p.Ala3709Gly
Search 100 bp 5'
Search 100 bp 3'