Canonical Allele Identifier: CA1693712928
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880938G= , CM000669.2:g.21880938G= GRCh38
NC_000007.13:g.21920556G= , CM000669.1:g.21920556G= GRCh37
NC_000007.12:g.21887081G= NCBI36
NG_012886.2:g.342724G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12387+45G= MANE Select ENSP00000475939.1:n.12387+45G=
ENST00000328843.10:c.12408+45G= ENSP00000330671.7:n.12408+45G=
ENST00000409508.7:c.12387+45G= ENSP00000475939.1:n.12387+45G=
ENST00000620169.4:c.12408+45G= ENSP00000481693.1:n.12408+45G=
NM_001277115.1:c.12387+45G= NP_001264044.1:n.12387+45G=
NM_001277115.2:c.12387+45G= MANE Select NP_001264044.1:n.12387+45G=