Canonical Allele Identifier: CA2681986976
Gene: DNAH11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748475_21748478del , CM000669.2:g.21748475_21748478del GRCh38
NC_000007.13:g.21788093_21788096del , CM000669.1:g.21788093_21788096del GRCh37
NC_000007.12:g.21754618_21754621del NCBI36
NG_012886.2:g.210261_210264del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8511-105_8511-102del MANE Select ENSP00000475939.1:n.8511-105_8511-102del
ENST00000328843.10:c.8532-105_8532-102del ENSP00000330671.7:n.8532-105_8532-102del
ENST00000409508.7:c.8511-105_8511-102del ENSP00000475939.1:n.8511-105_8511-102del
ENST00000620169.4:c.8532-105_8532-102del ENSP00000481693.1:n.8532-105_8532-102del
NM_001277115.1:c.8511-105_8511-102del NP_001264044.1:n.8511-105_8511-102del
NM_001277115.2:c.8511-105_8511-102del MANE Select NP_001264044.1:n.8511-105_8511-102del