Canonical Allele Identifier: CA1693712597

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21880717T= , CM000669.2:g.21880717T=	GRCh38
NC_000007.13:g.21920335T= , CM000669.1:g.21920335T=	GRCh37
NC_000007.12:g.21886860T=	NCBI36
NG_012886.2:g.342503T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.12211T= MANE Select	ENSP00000475939.1:p.Cys4071=
ENST00000328843.10:c.12232T=	ENSP00000330671.7:p.Cys4078=
ENST00000409508.7:c.12211T=	ENSP00000475939.1:p.Cys4071=
ENST00000620169.4:c.12232T=	ENSP00000481693.1:p.Cys4078=
NM_001277115.1:c.12211T=	NP_001264044.1:p.Cys4071=
NM_001277115.2:c.12211T= MANE Select	NP_001264044.1:p.Cys4071=