Canonical Allele Identifier: CA1693708801
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21854299T= , CM000669.2:g.21854299T= GRCh38
NC_000007.13:g.21893917T= , CM000669.1:g.21893917T= GRCh37
NC_000007.12:g.21860442T= NCBI36
NG_012886.2:g.316085T=

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11062-16T= MANE Select ENSP00000475939.1:n.11062-16T=
ENST00000328843.10:c.11083-16T= ENSP00000330671.7:n.11083-16T=
ENST00000409508.7:c.11062-16T= ENSP00000475939.1:n.11062-16T=
ENST00000421290.1:n.245-16T=
ENST00000607413.5:n.325-16T=
ENST00000620169.4:c.11083-16T= ENSP00000481693.1:n.11083-16T=
NM_001277115.1:c.11062-16T= NP_001264044.1:n.11062-16T=
NM_001277115.2:c.11062-16T= MANE Select NP_001264044.1:n.11062-16T=