Canonical Allele Identifier: CA1693713197

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21881244_21881245delinsAT , CM000669.2:g.21881244_21881245delinsAT	GRCh38
NC_000007.13:g.21920862_21920863delinsAT , CM000669.1:g.21920862_21920863delinsAT	GRCh37
NC_000007.12:g.21887387_21887388delinsAT	NCBI36
NG_012886.2:g.343030_343031delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12387+351_12387+352delinsAT MANE Select	ENSP00000475939.1:n.12387+351_12387+352delinsAT
ENST00000328843.10:c.12408+351_12408+352delinsAT	ENSP00000330671.7:n.12408+351_12408+352delinsAT
ENST00000409508.7:c.12387+351_12387+352delinsAT	ENSP00000475939.1:n.12387+351_12387+352delinsAT
ENST00000620169.4:c.12408+351_12408+352delinsAT	ENSP00000481693.1:n.12408+351_12408+352delinsAT
NM_001277115.1:c.12387+351_12387+352delinsAT	NP_001264044.1:n.12387+351_12387+352delinsAT
NM_001277115.2:c.12387+351_12387+352delinsAT MANE Select	NP_001264044.1:n.12387+351_12387+352delinsAT