Canonical Allele Identifier: CA155087083
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1796085
ClinVar RCV Id: RCV002441459
dbSNP Id: rs997071145

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21599914A>T , CM000669.2:g.21599914A>T GRCh38
NC_000007.13:g.21639532A>T , CM000669.1:g.21639532A>T GRCh37
NC_000007.12:g.21606057A>T NCBI36
NG_012886.2:g.61700A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.2795A>T MANE Select ENSP00000475939.1:p.Lys932Met
ENST00000328843.10:c.2795A>T ENSP00000330671.7:p.Lys932Met
ENST00000409508.7:c.2795A>T ENSP00000475939.1:p.Lys932Met
ENST00000620169.4:c.2795A>T ENSP00000481693.1:p.Lys932Met
NM_001277115.1:c.2795A>T NP_001264044.1:p.Lys932Met
NM_001277115.2:c.2795A>T MANE Select NP_001264044.1:p.Lys932Met