Canonical Allele Identifier: CA1693571413
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619077C= , CM000669.2:g.21619077C= GRCh38
NC_000007.13:g.21658695C= , CM000669.1:g.21658695C= GRCh37
NC_000007.12:g.21625220C= NCBI36
NG_012886.2:g.80863C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4255-23C= MANE Select ENSP00000475939.1:n.4255-23C=
ENST00000328843.10:c.4270-23C= ENSP00000330671.7:n.4270-23C=
ENST00000409508.7:c.4255-23C= ENSP00000475939.1:n.4255-23C=
ENST00000465593.1:n.281-23C=
ENST00000620169.4:c.4270-23C= ENSP00000481693.1:n.4270-23C=
NM_001277115.1:c.4255-23C= NP_001264044.1:n.4255-23C=
NM_001277115.2:c.4255-23C= MANE Select NP_001264044.1:n.4255-23C=