Canonical Allele Identifier: CA2681976624

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21558699-T-TAG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558699_21558700insAG , CM000669.2:g.21558699_21558700insAG	GRCh38
NC_000007.13:g.21598317_21598318insAG , CM000669.1:g.21598317_21598318insAG	GRCh37
NC_000007.12:g.21564842_21564843insAG	NCBI36
NG_012886.2:g.20485_20486insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-103_496-102insAG MANE Select	ENSP00000475939.1:n.496-103_496-102insAG
ENST00000328843.10:c.496-103_496-102insAG	ENSP00000330671.7:n.496-103_496-102insAG
ENST00000409508.7:c.496-103_496-102insAG	ENSP00000475939.1:n.496-103_496-102insAG
ENST00000620169.4:c.496-103_496-102insAG	ENSP00000481693.1:n.496-103_496-102insAG
NM_001277115.1:c.496-103_496-102insAG	NP_001264044.1:n.496-103_496-102insAG
NM_001277115.2:c.496-103_496-102insAG MANE Select	NP_001264044.1:n.496-103_496-102insAG