Canonical Allele Identifier: CA366959963
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs4722064

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21854375G>C , CM000669.2:g.21854375G>C GRCh38
NC_000007.13:g.21893993G>C , CM000669.1:g.21893993G>C GRCh37
NC_000007.12:g.21860518G>C NCBI36
NG_012886.2:g.316161G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11122G>C MANE Select ENSP00000475939.1:p.Val3708Leu
ENST00000328843.10:c.11143G>C ENSP00000330671.7:p.Val3715Leu
ENST00000409508.7:c.11122G>C ENSP00000475939.1:p.Val3708Leu
ENST00000421290.1:n.305G>C
ENST00000607413.5:n.385G>C
ENST00000620169.4:c.11143G>C ENSP00000481693.1:p.Val3715Leu
NM_001277115.1:c.11122G>C NP_001264044.1:p.Val3708Leu
NM_001277115.2:c.11122G>C MANE Select NP_001264044.1:p.Val3708Leu