Canonical Allele Identifier: CA2714084408
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs2128467406

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21664312_21664317dup , CM000669.2:g.21664312_21664317dup GRCh38
NC_000007.13:g.21703930_21703935dup , CM000669.1:g.21703930_21703935dup GRCh37
NC_000007.12:g.21670455_21670460dup NCBI36
NG_012886.2:g.126098_126103dup

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.5328+5281_5328+5286dup MANE Select ENSP00000475939.1:n.5328+5281_5328+5286du...
ENST00000328843.10:c.5343+5281_5343+5286dup ENSP00000330671.7:n.5343+5281_5343+5286du...
ENST00000409508.7:c.5328+5281_5328+5286dup ENSP00000475939.1:n.5328+5281_5328+5286du...
ENST00000620169.4:c.5343+5281_5343+5286dup ENSP00000481693.1:n.5343+5281_5343+5286du...
NM_001277115.1:c.5328+5281_5328+5286dup NP_001264044.1:n.5328+5281_5328+5286dup
NM_001277115.2:c.5328+5281_5328+5286dup MANE Select NP_001264044.1:n.5328+5281_5328+5286dup