Canonical Allele Identifier: CA2681990792

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21854291-TTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21854293_21854294del , CM000669.2:g.21854293_21854294del	GRCh38
NC_000007.13:g.21893911_21893912del , CM000669.1:g.21893911_21893912del	GRCh37
NC_000007.12:g.21860436_21860437del	NCBI36
NG_012886.2:g.316079_316080del

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.11062-22_11062-21del MANE Select	ENSP00000475939.1:n.11062-22_11062-21del
ENST00000328843.10:c.11083-22_11083-21del	ENSP00000330671.7:n.11083-22_11083-21del
ENST00000409508.7:c.11062-22_11062-21del	ENSP00000475939.1:n.11062-22_11062-21del
ENST00000421290.1:n.245-22_245-21del
ENST00000607413.5:n.325-22_325-21del
ENST00000620169.4:c.11083-22_11083-21del	ENSP00000481693.1:n.11083-22_11083-21del
NM_001277115.1:c.11062-22_11062-21del	NP_001264044.1:n.11062-22_11062-21del
NM_001277115.2:c.11062-22_11062-21del MANE Select	NP_001264044.1:n.11062-22_11062-21del