Canonical Allele Identifier: CA2681990791
Gene: DNAH11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21854290_21854293del , CM000669.2:g.21854290_21854293del GRCh38
NC_000007.13:g.21893908_21893911del , CM000669.1:g.21893908_21893911del GRCh37
NC_000007.12:g.21860433_21860436del NCBI36
NG_012886.2:g.316076_316079del

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11062-25_11062-22del MANE Select ENSP00000475939.1:n.11062-25_11062-22del
ENST00000328843.10:c.11083-25_11083-22del ENSP00000330671.7:n.11083-25_11083-22del
ENST00000409508.7:c.11062-25_11062-22del ENSP00000475939.1:n.11062-25_11062-22del
ENST00000421290.1:n.245-25_245-22del
ENST00000607413.5:n.325-25_325-22del
ENST00000620169.4:c.11083-25_11083-22del ENSP00000481693.1:n.11083-25_11083-22del
NM_001277115.1:c.11062-25_11062-22del NP_001264044.1:n.11062-25_11062-22del
NM_001277115.2:c.11062-25_11062-22del MANE Select NP_001264044.1:n.11062-25_11062-22del