Canonical Allele Identifier: CA453965801
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21893957A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21854339A>C , CM000669.2:g.21854339A>C GRCh38
NC_000007.13:g.21893957A>C , CM000669.1:g.21893957A>C GRCh37
NC_000007.12:g.21860482A>C NCBI36
NG_012886.2:g.316125A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.11086A>C MANE Select ENSP00000475939.1:p.Arg3696=
ENST00000328843.10:c.11107A>C ENSP00000330671.7:p.Arg3703=
ENST00000409508.7:c.11086A>C ENSP00000475939.1:p.Arg3696=
ENST00000421290.1:n.269A>C
ENST00000607413.5:n.349A>C
ENST00000620169.4:c.11107A>C ENSP00000481693.1:p.Arg3703=
NM_001277115.1:c.11086A>C NP_001264044.1:p.Arg3696=
NM_001277115.2:c.11086A>C MANE Select NP_001264044.1:p.Arg3696=
Search 100 bp 5'
Search 100 bp 3'