Canonical Allele Identifier: CA1693666595
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816705A= , CM000669.2:g.21816705A= GRCh38
NC_000007.13:g.21856323A= , CM000669.1:g.21856323A= GRCh37
NC_000007.12:g.21822848A= NCBI36
NG_012886.2:g.278491A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10568+3A= MANE Select ENSP00000475939.1:n.10568+3A=
ENST00000328843.10:c.10589+3A= ENSP00000330671.7:n.10589+3A=
ENST00000409508.7:c.10568+3A= ENSP00000475939.1:n.10568+3A=
ENST00000620169.4:c.10589+3A= ENSP00000481693.1:n.10589+3A=
NM_001277115.1:c.10568+3A= NP_001264044.1:n.10568+3A=
NM_001277115.2:c.10568+3A= MANE Select NP_001264044.1:n.10568+3A=