Canonical Allele Identifier: CA155122058
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs769651483

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816477C>A , CM000669.2:g.21816477C>A GRCh38
NC_000007.13:g.21856095C>A , CM000669.1:g.21856095C>A GRCh37
NC_000007.12:g.21822620C>A NCBI36
NG_012886.2:g.278263C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10343C>A MANE Select ENSP00000475939.1:p.Pro3448Gln
ENST00000328843.10:c.10364C>A ENSP00000330671.7:p.Pro3455Gln
ENST00000409508.7:c.10343C>A ENSP00000475939.1:p.Pro3448Gln
ENST00000620169.4:c.10364C>A ENSP00000481693.1:p.Pro3455Gln
NM_001277115.1:c.10343C>A NP_001264044.1:p.Pro3448Gln
NM_001277115.2:c.10343C>A MANE Select NP_001264044.1:p.Pro3448Gln