Canonical Allele Identifier: CA453967863
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2698670
ClinVar RCV Id: RCV003536179
MyVariant Identifiers: chr7:g.21920376C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880758C>G , CM000669.2:g.21880758C>G GRCh38
NC_000007.13:g.21920376C>G , CM000669.1:g.21920376C>G GRCh37
NC_000007.12:g.21886901C>G NCBI36
NG_012886.2:g.342544C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12252C>G MANE Select ENSP00000475939.1:p.Leu4084=
ENST00000328843.10:c.12273C>G ENSP00000330671.7:p.Leu4091=
ENST00000409508.7:c.12252C>G ENSP00000475939.1:p.Leu4084=
ENST00000620169.4:c.12273C>G ENSP00000481693.1:p.Leu4091=
NM_001277115.1:c.12252C>G NP_001264044.1:p.Leu4084=
NM_001277115.2:c.12252C>G MANE Select NP_001264044.1:p.Leu4084=