Canonical Allele Identifier: CA1693537968
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21543348C= , CM000669.2:g.21543348C= GRCh38
NC_000007.13:g.21582966C= , CM000669.1:g.21582966C= GRCh37
NC_000007.12:g.21549491C= NCBI36
NG_012886.2:g.5134C=

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.103C= MANE Select ENSP00000475939.1:p.Leu35=
ENST00000328843.10:c.103C= ENSP00000330671.7:p.Leu35=
ENST00000409508.7:c.103C= ENSP00000475939.1:p.Leu35=
ENST00000620169.4:c.103C= ENSP00000481693.1:p.Leu35=
NM_001277115.1:c.103C= NP_001264044.1:p.Leu35=
NM_001277115.2:c.103C= MANE Select NP_001264044.1:p.Leu35=