Canonical Allele Identifier: CA1693537973
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21543350C= , CM000669.2:g.21543350C= GRCh38
NC_000007.13:g.21582968C= , CM000669.1:g.21582968C= GRCh37
NC_000007.12:g.21549493C= NCBI36
NG_012886.2:g.5136C=

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.105C= MANE Select ENSP00000475939.1:p.Leu35=
ENST00000328843.10:c.105C= ENSP00000330671.7:p.Leu35=
ENST00000409508.7:c.105C= ENSP00000475939.1:p.Leu35=
ENST00000620169.4:c.105C= ENSP00000481693.1:p.Leu35=
NM_001277115.1:c.105C= NP_001264044.1:p.Leu35=
NM_001277115.2:c.105C= MANE Select NP_001264044.1:p.Leu35=