Canonical Allele Identifier: CA4182625
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs754541157
gnomAD v2: 7-21894002-A-G
gnomAD v4: 7-21854384-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21854384A>G , CM000669.2:g.21854384A>G GRCh38
NC_000007.13:g.21894002A>G , CM000669.1:g.21894002A>G GRCh37
NC_000007.12:g.21860527A>G NCBI36
NG_012886.2:g.316170A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11131A>G MANE Select ENSP00000475939.1:p.Arg3711Gly
ENST00000328843.10:c.11152A>G ENSP00000330671.7:p.Arg3718Gly
ENST00000409508.7:c.11131A>G ENSP00000475939.1:p.Arg3711Gly
ENST00000421290.1:n.314A>G
ENST00000607413.5:n.394A>G
ENST00000620169.4:c.11152A>G ENSP00000481693.1:p.Arg3718Gly
NM_001277115.1:c.11131A>G NP_001264044.1:p.Arg3711Gly
NM_001277115.2:c.11131A>G MANE Select NP_001264044.1:p.Arg3711Gly