Canonical Allele Identifier: CA1693712850
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880872_21880873delinsCT , CM000669.2:g.21880872_21880873delinsCT GRCh38
NC_000007.13:g.21920490_21920491delinsCT , CM000669.1:g.21920490_21920491delinsCT GRCh37
NC_000007.12:g.21887015_21887016delinsCT NCBI36
NG_012886.2:g.342658_342659delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12366_12367delinsCT MANE Select ENSP00000475939.1:p.Asn4122=
ENST00000328843.10:c.12387_12388delinsCT ENSP00000330671.7:p.Asn4129=
ENST00000409508.7:c.12366_12367delinsCT ENSP00000475939.1:p.Asn4122=
ENST00000620169.4:c.12387_12388delinsCT ENSP00000481693.1:p.Asn4129=
NM_001277115.1:c.12366_12367delinsCT NP_001264044.1:p.Asn4122=
NM_001277115.2:c.12366_12367delinsCT MANE Select NP_001264044.1:p.Asn4122=
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