Canonical Allele Identifier: CA453968626
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21788357T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748739T>G , CM000669.2:g.21748739T>G GRCh38
NC_000007.13:g.21788357T>G , CM000669.1:g.21788357T>G GRCh37
NC_000007.12:g.21754882T>G NCBI36
NG_012886.2:g.210525T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8670T>G MANE Select ENSP00000475939.1:p.Leu2890=
ENST00000328843.10:c.8691T>G ENSP00000330671.7:p.Leu2897=
ENST00000409508.7:c.8670T>G ENSP00000475939.1:p.Leu2890=
ENST00000620169.4:c.8691T>G ENSP00000481693.1:p.Leu2897=
NM_001277115.1:c.8670T>G NP_001264044.1:p.Leu2890=
NM_001277115.2:c.8670T>G MANE Select NP_001264044.1:p.Leu2890=