Canonical Allele Identifier: CA1693708800
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21854298G= , CM000669.2:g.21854298G= GRCh38
NC_000007.13:g.21893916G= , CM000669.1:g.21893916G= GRCh37
NC_000007.12:g.21860441G= NCBI36
NG_012886.2:g.316084G=

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11062-17G= MANE Select ENSP00000475939.1:n.11062-17G=
ENST00000328843.10:c.11083-17G= ENSP00000330671.7:n.11083-17G=
ENST00000409508.7:c.11062-17G= ENSP00000475939.1:n.11062-17G=
ENST00000421290.1:n.245-17G=
ENST00000607413.5:n.325-17G=
ENST00000620169.4:c.11083-17G= ENSP00000481693.1:n.11083-17G=
NM_001277115.1:c.11062-17G= NP_001264044.1:n.11062-17G=
NM_001277115.2:c.11062-17G= MANE Select NP_001264044.1:n.11062-17G=