Canonical Allele Identifier: CA366948804
Gene: DNAH11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816621T>A , CM000669.2:g.21816621T>A GRCh38
NC_000007.13:g.21856239T>A , CM000669.1:g.21856239T>A GRCh37
NC_000007.12:g.21822764T>A NCBI36
NG_012886.2:g.278407T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10487T>A MANE Select ENSP00000475939.1:p.Ile3496Lys
ENST00000328843.10:c.10508T>A ENSP00000330671.7:p.Ile3503Lys
ENST00000409508.7:c.10487T>A ENSP00000475939.1:p.Ile3496Lys
ENST00000620169.4:c.10508T>A ENSP00000481693.1:p.Ile3503Lys
NM_001277115.1:c.10487T>A NP_001264044.1:p.Ile3496Lys
NM_001277115.2:c.10487T>A MANE Select NP_001264044.1:p.Ile3496Lys