Canonical Allele Identifier: CA1693538846

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558639_21558640delinsAT , CM000669.2:g.21558639_21558640delinsAT	GRCh38
NC_000007.13:g.21598257_21598258delinsAT , CM000669.1:g.21598257_21598258delinsAT	GRCh37
NC_000007.12:g.21564782_21564783delinsAT	NCBI36
NG_012886.2:g.20425_20426delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-163_496-162delinsAT MANE Select	ENSP00000475939.1:n.496-163_496-162delinsAT
ENST00000328843.10:c.496-163_496-162delinsAT	ENSP00000330671.7:n.496-163_496-162delinsAT
ENST00000409508.7:c.496-163_496-162delinsAT	ENSP00000475939.1:n.496-163_496-162delinsAT
ENST00000620169.4:c.496-163_496-162delinsAT	ENSP00000481693.1:n.496-163_496-162delinsAT
NM_001277115.1:c.496-163_496-162delinsAT	NP_001264044.1:n.496-163_496-162delinsAT
NM_001277115.2:c.496-163_496-162delinsAT MANE Select	NP_001264044.1:n.496-163_496-162delinsAT