Canonical Allele Identifier: CA2681976770

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21559120-TCAAGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21559122_21559126del , CM000669.2:g.21559122_21559126del	GRCh38
NC_000007.13:g.21598740_21598744del , CM000669.1:g.21598740_21598744del	GRCh37
NC_000007.12:g.21565265_21565269del	NCBI36
NG_012886.2:g.20908_20912del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.692+124_692+128del MANE Select	ENSP00000475939.1:n.692+124_692+128del
ENST00000328843.10:c.692+124_692+128del	ENSP00000330671.7:n.692+124_692+128del
ENST00000409508.7:c.692+124_692+128del	ENSP00000475939.1:n.692+124_692+128del
ENST00000620169.4:c.692+124_692+128del	ENSP00000481693.1:n.692+124_692+128del
NM_001277115.1:c.692+124_692+128del	NP_001264044.1:n.692+124_692+128del
NM_001277115.2:c.692+124_692+128del MANE Select	NP_001264044.1:n.692+124_692+128del