Canonical Allele Identifier: CA2681975850
Gene: DNAH11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21543244del , CM000669.2:g.21543244del GRCh38
NC_000007.13:g.21582862del , CM000669.1:g.21582862del GRCh37
NC_000007.12:g.21549387del NCBI36
NG_012886.2:g.5030del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.-2del MANE Select ENSP00000475939.1:n.-2del
ENST00000328843.10:c.-2del ENSP00000330671.7:n.-2del
ENST00000409508.7:c.-2del ENSP00000475939.1:n.-2del
ENST00000620169.4:c.-2del ENSP00000481693.1:n.-2del
NM_001277115.1:c.-2del NP_001264044.1:n.-2del
NM_001277115.2:c.-2del MANE Select NP_001264044.1:n.-2del