Canonical Allele Identifier: CA1693713095

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21881124_21881125delinsTA , CM000669.2:g.21881124_21881125delinsTA	GRCh38
NC_000007.13:g.21920742_21920743delinsTA , CM000669.1:g.21920742_21920743delinsTA	GRCh37
NC_000007.12:g.21887267_21887268delinsTA	NCBI36
NG_012886.2:g.342910_342911delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12387+231_12387+232delinsTA MANE Select	ENSP00000475939.1:n.12387+231_12387+232delinsTA
ENST00000328843.10:c.12408+231_12408+232delinsTA	ENSP00000330671.7:n.12408+231_12408+232delinsTA
ENST00000409508.7:c.12387+231_12387+232delinsTA	ENSP00000475939.1:n.12387+231_12387+232delinsTA
ENST00000620169.4:c.12408+231_12408+232delinsTA	ENSP00000481693.1:n.12408+231_12408+232delinsTA
NM_001277115.1:c.12387+231_12387+232delinsTA	NP_001264044.1:n.12387+231_12387+232delinsTA
NM_001277115.2:c.12387+231_12387+232delinsTA MANE Select	NP_001264044.1:n.12387+231_12387+232delinsTA