Canonical Allele Identifier: CA1693624672

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21704463T= , CM000669.2:g.21704463T=	GRCh38
NC_000007.13:g.21744081T= , CM000669.1:g.21744081T=	GRCh37
NC_000007.12:g.21710606T=	NCBI36
NG_012886.2:g.166249T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.6303T= MANE Select	ENSP00000475939.1:p.Asn2101=
ENST00000328843.10:c.6324T=	ENSP00000330671.7:p.Asn2108=
ENST00000409508.7:c.6303T=	ENSP00000475939.1:p.Asn2101=
ENST00000620169.4:c.6324T=	ENSP00000481693.1:p.Asn2108=
NM_001277115.1:c.6303T=	NP_001264044.1:p.Asn2101=
NM_001277115.2:c.6303T= MANE Select	NP_001264044.1:p.Asn2101=