Canonical Allele Identifier: CA1693666066

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816416_21816418delinsTTC , CM000669.2:g.21816416_21816418delinsTTC	GRCh38
NC_000007.13:g.21856034_21856036delinsTTC , CM000669.1:g.21856034_21856036delinsTTC	GRCh37
NC_000007.12:g.21822559_21822561delinsTTC	NCBI36
NG_012886.2:g.278202_278204delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10333-51_10333-49delinsTTC MANE Select	ENSP00000475939.1:n.10333-51_10333-49delinsTTC
ENST00000328843.10:c.10354-51_10354-49delinsTTC	ENSP00000330671.7:n.10354-51_10354-49delinsTTC
ENST00000409508.7:c.10333-51_10333-49delinsTTC	ENSP00000475939.1:n.10333-51_10333-49delinsTTC
ENST00000620169.4:c.10354-51_10354-49delinsTTC	ENSP00000481693.1:n.10354-51_10354-49delinsTTC
NM_001277115.1:c.10333-51_10333-49delinsTTC	NP_001264044.1:n.10333-51_10333-49delinsTTC
NM_001277115.2:c.10333-51_10333-49delinsTTC MANE Select	NP_001264044.1:n.10333-51_10333-49delinsTTC