Canonical Allele Identifier: CA1693712893
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880901C= , CM000669.2:g.21880901C= GRCh38
NC_000007.13:g.21920519C= , CM000669.1:g.21920519C= GRCh37
NC_000007.12:g.21887044C= NCBI36
NG_012886.2:g.342687C=

Transcript Alleles

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