Canonical Allele Identifier: CA1693662157
Gene: DNAH11 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748751A= , CM000669.2:g.21748751A= GRCh38
NC_000007.13:g.21788369A= , CM000669.1:g.21788369A= GRCh37
NC_000007.12:g.21754894A= NCBI36
NG_012886.2:g.210537A=

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.8673+9A= MANE Select ENSP00000475939.1:n.8673+9A=
ENST00000328843.10:c.8694+9A= ENSP00000330671.7:n.8694+9A=
ENST00000409508.7:c.8673+9A= ENSP00000475939.1:n.8673+9A=
ENST00000620169.4:c.8694+9A= ENSP00000481693.1:n.8694+9A=
NM_001277115.1:c.8673+9A= NP_001264044.1:n.8673+9A=
NM_001277115.2:c.8673+9A= MANE Select NP_001264044.1:n.8673+9A=
Search 100 bp 5'
Search 100 bp 3'