Canonical Allele Identifier: CA155074168

Gene: DNAH11

Linked Data

• dbSNP Id: rs72555812
• MyVariant Identifiers: chr7:g.21598314_21598315insGAT (hg19) ; chr7:g.21558696_21558697insGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558696_21558697insGAT , CM000669.2:g.21558696_21558697insGAT	GRCh38
NC_000007.13:g.21598314_21598315insGAT , CM000669.1:g.21598314_21598315insGAT	GRCh37
NC_000007.12:g.21564839_21564840insGAT	NCBI36
NG_012886.2:g.20482_20483insGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-106_496-105insGAT MANE Select	ENSP00000475939.1:n.496-106_496-105insGAT
ENST00000328843.10:c.496-106_496-105insGAT	ENSP00000330671.7:n.496-106_496-105insGAT
ENST00000409508.7:c.496-106_496-105insGAT	ENSP00000475939.1:n.496-106_496-105insGAT
ENST00000620169.4:c.496-106_496-105insGAT	ENSP00000481693.1:n.496-106_496-105insGAT
NM_001277115.1:c.496-106_496-105insGAT	NP_001264044.1:n.496-106_496-105insGAT
NM_001277115.2:c.496-106_496-105insGAT MANE Select	NP_001264044.1:n.496-106_496-105insGAT