Canonical Allele Identifier: CA1693661755

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21748521_21748524delinsCAGA , CM000669.2:g.21748521_21748524delinsCAGA	GRCh38
NC_000007.13:g.21788139_21788142delinsCAGA , CM000669.1:g.21788139_21788142delinsCAGA	GRCh37
NC_000007.12:g.21754664_21754667delinsCAGA	NCBI36
NG_012886.2:g.210307_210310delinsCAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.8511-59_8511-56delinsCAGA MANE Select	ENSP00000475939.1:n.8511-59_8511-56delinsCAGA
ENST00000328843.10:c.8532-59_8532-56delinsCAGA	ENSP00000330671.7:n.8532-59_8532-56delinsCAGA
ENST00000409508.7:c.8511-59_8511-56delinsCAGA	ENSP00000475939.1:n.8511-59_8511-56delinsCAGA
ENST00000620169.4:c.8532-59_8532-56delinsCAGA	ENSP00000481693.1:n.8532-59_8532-56delinsCAGA
NM_001277115.1:c.8511-59_8511-56delinsCAGA	NP_001264044.1:n.8511-59_8511-56delinsCAGA
NM_001277115.2:c.8511-59_8511-56delinsCAGA MANE Select	NP_001264044.1:n.8511-59_8511-56delinsCAGA