Canonical Allele Identifier: CA1693538941

Gene: DNAH11

Linked Data

• dbSNP Id: rs1783319611
• gnomAD v4: 7-21558715-GTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558718_21558719del , CM000669.2:g.21558718_21558719del	GRCh38
NC_000007.13:g.21598336_21598337del , CM000669.1:g.21598336_21598337del	GRCh37
NC_000007.12:g.21564861_21564862del	NCBI36
NG_012886.2:g.20504_20505del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-84_496-83del MANE Select	ENSP00000475939.1:n.496-84_496-83del
ENST00000328843.10:c.496-84_496-83del	ENSP00000330671.7:n.496-84_496-83del
ENST00000409508.7:c.496-84_496-83del	ENSP00000475939.1:n.496-84_496-83del
ENST00000620169.4:c.496-84_496-83del	ENSP00000481693.1:n.496-84_496-83del
NM_001277115.1:c.496-84_496-83del	NP_001264044.1:n.496-84_496-83del
NM_001277115.2:c.496-84_496-83del MANE Select	NP_001264044.1:n.496-84_496-83del