Canonical Allele Identifier: CA1693661677
Gene: DNAH11 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748471A= , CM000669.2:g.21748471A= GRCh38
NC_000007.13:g.21788089A= , CM000669.1:g.21788089A= GRCh37
NC_000007.12:g.21754614A= NCBI36
NG_012886.2:g.210257A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8511-109A= MANE Select ENSP00000475939.1:n.8511-109A=
ENST00000328843.10:c.8532-109A= ENSP00000330671.7:n.8532-109A=
ENST00000409508.7:c.8511-109A= ENSP00000475939.1:n.8511-109A=
ENST00000620169.4:c.8532-109A= ENSP00000481693.1:n.8532-109A=
NM_001277115.1:c.8511-109A= NP_001264044.1:n.8511-109A=
NM_001277115.2:c.8511-109A= MANE Select NP_001264044.1:n.8511-109A=
Search 100 bp 5'
Search 100 bp 3'