Canonical Allele Identifier: CA1693579042

Gene: DNAH11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21599858_21599859delinsCA , CM000669.2:g.21599858_21599859delinsCA	GRCh38
NC_000007.13:g.21639476_21639477delinsCA , CM000669.1:g.21639476_21639477delinsCA	GRCh37
NC_000007.12:g.21606001_21606002delinsCA	NCBI36
NG_012886.2:g.61644_61645delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.2739_2740delinsCA MANE Select	ENSP00000475939.1:p.Asp913=
ENST00000328843.10:c.2739_2740delinsCA	ENSP00000330671.7:p.Asp913=
ENST00000409508.7:c.2739_2740delinsCA	ENSP00000475939.1:p.Asp913=
ENST00000620169.4:c.2739_2740delinsCA	ENSP00000481693.1:p.Asp913=
NM_001277115.1:c.2739_2740delinsCA	NP_001264044.1:p.Asp913=
NM_001277115.2:c.2739_2740delinsCA MANE Select	NP_001264044.1:p.Asp913=