Canonical Allele Identifier: CA1693557452
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21567605C= , CM000669.2:g.21567605C= GRCh38
NC_000007.13:g.21607223C= , CM000669.1:g.21607223C= GRCh37
NC_000007.12:g.21573748C= NCBI36
NG_012886.2:g.29391C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.1195-2464C= MANE Select ENSP00000475939.1:n.1195-2464C=
ENST00000328843.10:c.1195-2464C= ENSP00000330671.7:n.1195-2464C=
ENST00000409508.7:c.1195-2464C= ENSP00000475939.1:n.1195-2464C=
ENST00000496218.1:n.81-2464C=
ENST00000620169.4:c.1195-2464C= ENSP00000481693.1:n.1195-2464C=
NM_001277115.1:c.1195-2464C= NP_001264044.1:n.1195-2464C=
XR_927090.1:n.563+5721G=
XR_001745114.1:n.2793+5721G=
NM_001277115.2:c.1195-2464C= MANE Select NP_001264044.1:n.1195-2464C=