Canonical Allele Identifier: CA1693722433

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21864577T= , CM000669.2:g.21864577T=	GRCh38
NC_000007.13:g.21904195T= , CM000669.1:g.21904195T=	GRCh37
NC_000007.12:g.21870720T=	NCBI36
NG_012886.2:g.326363T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.11416T= MANE Select	ENSP00000475939.1:p.Phe3806=
ENST00000328843.10:c.11437T=	ENSP00000330671.7:p.Phe3813=
ENST00000409508.7:c.11416T=	ENSP00000475939.1:p.Phe3806=
ENST00000620169.4:c.11437T=	ENSP00000481693.1:p.Phe3813=
NM_001277115.1:c.11416T=	NP_001264044.1:p.Phe3806=
NM_001277115.2:c.11416T= MANE Select	NP_001264044.1:p.Phe3806=