Canonical Allele Identifier: CA1693571550

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21619134C= , CM000669.2:g.21619134C=	GRCh38
NC_000007.13:g.21658752C= , CM000669.1:g.21658752C=	GRCh37
NC_000007.12:g.21625277C=	NCBI36
NG_012886.2:g.80920C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.4289C= MANE Select	ENSP00000475939.1:p.Ala1430=
ENST00000328843.10:c.4304C=	ENSP00000330671.7:p.Ala1435=
ENST00000409508.7:c.4289C=	ENSP00000475939.1:p.Ala1430=
ENST00000465593.1:n.315C=
ENST00000620169.4:c.4304C=	ENSP00000481693.1:p.Ala1435=
NM_001277115.1:c.4289C=	NP_001264044.1:p.Ala1430=
NM_001277115.2:c.4289C= MANE Select	NP_001264044.1:p.Ala1430=