Canonical Allele Identifier: CA1693709000

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21854379C= , CM000669.2:g.21854379C=	GRCh38
NC_000007.13:g.21893997C= , CM000669.1:g.21893997C=	GRCh37
NC_000007.12:g.21860522C=	NCBI36
NG_012886.2:g.316165C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.11126C= MANE Select	ENSP00000475939.1:p.Ala3709=
ENST00000328843.10:c.11147C=	ENSP00000330671.7:p.Ala3716=
ENST00000409508.7:c.11126C=	ENSP00000475939.1:p.Ala3709=
ENST00000421290.1:n.309C=
ENST00000607413.5:n.389C=
ENST00000620169.4:c.11147C=	ENSP00000481693.1:p.Ala3716=
NM_001277115.1:c.11126C=	NP_001264044.1:p.Ala3709=
NM_001277115.2:c.11126C= MANE Select	NP_001264044.1:p.Ala3709=