Canonical Allele Identifier: CA2681976620

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21558697-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558697_21558698insG , CM000669.2:g.21558697_21558698insG	GRCh38
NC_000007.13:g.21598315_21598316insG , CM000669.1:g.21598315_21598316insG	GRCh37
NC_000007.12:g.21564840_21564841insG	NCBI36
NG_012886.2:g.20483_20484insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-105_496-104insG MANE Select	ENSP00000475939.1:n.496-105_496-104insG
ENST00000328843.10:c.496-105_496-104insG	ENSP00000330671.7:n.496-105_496-104insG
ENST00000409508.7:c.496-105_496-104insG	ENSP00000475939.1:n.496-105_496-104insG
ENST00000620169.4:c.496-105_496-104insG	ENSP00000481693.1:n.496-105_496-104insG
NM_001277115.1:c.496-105_496-104insG	NP_001264044.1:n.496-105_496-104insG
NM_001277115.2:c.496-105_496-104insG MANE Select	NP_001264044.1:n.496-105_496-104insG