Canonical Allele Identifier: CA1693713187

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21881231_21881232delinsAT , CM000669.2:g.21881231_21881232delinsAT	GRCh38
NC_000007.13:g.21920849_21920850delinsAT , CM000669.1:g.21920849_21920850delinsAT	GRCh37
NC_000007.12:g.21887374_21887375delinsAT	NCBI36
NG_012886.2:g.343017_343018delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12387+338_12387+339delinsAT MANE Select	ENSP00000475939.1:n.12387+338_12387+339delinsAT
ENST00000328843.10:c.12408+338_12408+339delinsAT	ENSP00000330671.7:n.12408+338_12408+339delinsAT
ENST00000409508.7:c.12387+338_12387+339delinsAT	ENSP00000475939.1:n.12387+338_12387+339delinsAT
ENST00000620169.4:c.12408+338_12408+339delinsAT	ENSP00000481693.1:n.12408+338_12408+339delinsAT
NM_001277115.1:c.12387+338_12387+339delinsAT	NP_001264044.1:n.12387+338_12387+339delinsAT
NM_001277115.2:c.12387+338_12387+339delinsAT MANE Select	NP_001264044.1:n.12387+338_12387+339delinsAT