Canonical Allele Identifier: CA1099205709

Gene: DNAH11

Linked Data

• gnomAD v3: 7-21567652-T-TA
• gnomAD v4: 7-21567652-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21567652_21567653insA , CM000669.2:g.21567652_21567653insA	GRCh38
NC_000007.13:g.21607270_21607271insA , CM000669.1:g.21607270_21607271insA	GRCh37
NC_000007.12:g.21573795_21573796insA	NCBI36
NG_012886.2:g.29438_29439insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.1195-2417_1195-2416insA MANE Select	ENSP00000475939.1:n.1195-2417_1195-2416in...
ENST00000328843.10:c.1195-2417_1195-2416insA	ENSP00000330671.7:n.1195-2417_1195-2416in...
ENST00000409508.7:c.1195-2417_1195-2416insA	ENSP00000475939.1:n.1195-2417_1195-2416in...
ENST00000496218.1:n.81-2417_81-2416insA
ENST00000620169.4:c.1195-2417_1195-2416insA	ENSP00000481693.1:n.1195-2417_1195-2416in...
NM_001277115.1:c.1195-2417_1195-2416insA	NP_001264044.1:n.1195-2417_1195-2416insA
XR_927090.1:n.563+5673_563+5674insT
XR_001745114.1:n.2793+5673_2793+5674insT
NM_001277115.2:c.1195-2417_1195-2416insA MANE Select	NP_001264044.1:n.1195-2417_1195-2416insA