Canonical Allele Identifier: CA2681992319

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21880943-C-CAGTCTTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21880944_21880951dup , CM000669.2:g.21880944_21880951dup	GRCh38
NC_000007.13:g.21920562_21920569dup , CM000669.1:g.21920562_21920569dup	GRCh37
NC_000007.12:g.21887087_21887094dup	NCBI36
NG_012886.2:g.342730_342737dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.12387+51_12387+58dup MANE Select	ENSP00000475939.1:n.12387+51_12387+58dup
ENST00000328843.10:c.12408+51_12408+58dup	ENSP00000330671.7:n.12408+51_12408+58dup
ENST00000409508.7:c.12387+51_12387+58dup	ENSP00000475939.1:n.12387+51_12387+58dup
ENST00000620169.4:c.12408+51_12408+58dup	ENSP00000481693.1:n.12408+51_12408+58dup
NM_001277115.1:c.12387+51_12387+58dup	NP_001264044.1:n.12387+51_12387+58dup
NM_001277115.2:c.12387+51_12387+58dup MANE Select	NP_001264044.1:n.12387+51_12387+58dup