Canonical Allele Identifier: CA1693666004

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816322_21816323delinsGT , CM000669.2:g.21816322_21816323delinsGT	GRCh38
NC_000007.13:g.21855940_21855941delinsGT , CM000669.1:g.21855940_21855941delinsGT	GRCh37
NC_000007.12:g.21822465_21822466delinsGT	NCBI36
NG_012886.2:g.278108_278109delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10333-145_10333-144delinsGT MANE Select	ENSP00000475939.1:n.10333-145_10333-144delinsGT
ENST00000328843.10:c.10354-145_10354-144delinsGT	ENSP00000330671.7:n.10354-145_10354-144delinsGT
ENST00000409508.7:c.10333-145_10333-144delinsGT	ENSP00000475939.1:n.10333-145_10333-144delinsGT
ENST00000620169.4:c.10354-145_10354-144delinsGT	ENSP00000481693.1:n.10354-145_10354-144delinsGT
NM_001277115.1:c.10333-145_10333-144delinsGT	NP_001264044.1:n.10333-145_10333-144delinsGT
NM_001277115.2:c.10333-145_10333-144delinsGT MANE Select	NP_001264044.1:n.10333-145_10333-144delinsGT