Canonical Allele Identifier: CA1693571237

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21618943_21618944delinsAG , CM000669.2:g.21618943_21618944delinsAG	GRCh38
NC_000007.13:g.21658561_21658562delinsAG , CM000669.1:g.21658561_21658562delinsAG	GRCh37
NC_000007.12:g.21625086_21625087delinsAG	NCBI36
NG_012886.2:g.80729_80730delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.4255-157_4255-156delinsAG MANE Select	ENSP00000475939.1:n.4255-157_4255-156delinsAG
ENST00000328843.10:c.4270-157_4270-156delinsAG	ENSP00000330671.7:n.4270-157_4270-156delinsAG
ENST00000409508.7:c.4255-157_4255-156delinsAG	ENSP00000475939.1:n.4255-157_4255-156delinsAG
ENST00000465593.1:n.281-157_281-156delinsAG
ENST00000620169.4:c.4270-157_4270-156delinsAG	ENSP00000481693.1:n.4270-157_4270-156delinsAG
NM_001277115.1:c.4255-157_4255-156delinsAG	NP_001264044.1:n.4255-157_4255-156delinsAG
NM_001277115.2:c.4255-157_4255-156delinsAG MANE Select	NP_001264044.1:n.4255-157_4255-156delinsAG