Canonical Allele Identifier: CA453966578
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21856132G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816514G>C , CM000669.2:g.21816514G>C GRCh38
NC_000007.13:g.21856132G>C , CM000669.1:g.21856132G>C GRCh37
NC_000007.12:g.21822657G>C NCBI36
NG_012886.2:g.278300G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10380G>C MANE Select ENSP00000475939.1:p.Thr3460=
ENST00000328843.10:c.10401G>C ENSP00000330671.7:p.Thr3467=
ENST00000409508.7:c.10380G>C ENSP00000475939.1:p.Thr3460=
ENST00000620169.4:c.10401G>C ENSP00000481693.1:p.Thr3467=
NM_001277115.1:c.10380G>C NP_001264044.1:p.Thr3460=
NM_001277115.2:c.10380G>C MANE Select NP_001264044.1:p.Thr3460=
Search 100 bp 5'
Search 100 bp 3'