Canonical Allele Identifier: CA1693712544
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880683_21880688delinsTTCTTC , CM000669.2:g.21880683_21880688delinsTTCTTC GRCh38
NC_000007.13:g.21920301_21920306delinsTTCTTC , CM000669.1:g.21920301_21920306delinsTTCTTC GRCh37
NC_000007.12:g.21886826_21886831delinsTTCTTC NCBI36
NG_012886.2:g.342469_342474delinsTTCTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12196-19_12196-14delinsTTCTTC MANE Select ENSP00000475939.1:n.12196-19_12196-14delinsTTCTTC
ENST00000328843.10:c.12217-19_12217-14delinsTTCTTC ENSP00000330671.7:n.12217-19_12217-14delinsTTCTTC
ENST00000409508.7:c.12196-19_12196-14delinsTTCTTC ENSP00000475939.1:n.12196-19_12196-14delinsTTCTTC
ENST00000620169.4:c.12217-19_12217-14delinsTTCTTC ENSP00000481693.1:n.12217-19_12217-14delinsTTCTTC
NM_001277115.1:c.12196-19_12196-14delinsTTCTTC NP_001264044.1:n.12196-19_12196-14delinsTTCTTC
NM_001277115.2:c.12196-19_12196-14delinsTTCTTC MANE Select NP_001264044.1:n.12196-19_12196-14delinsTTCTTC