Canonical Allele Identifier: CA1099205699

Gene: DNAH11

Linked Data

• gnomAD v3: 7-21567645-T-TCGGTGG
• gnomAD v4: 7-21567645-T-TCGGTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21567645_21567646insCGGTGG , CM000669.2:g.21567645_21567646insCGGTGG	GRCh38
NC_000007.13:g.21607263_21607264insCGGTGG , CM000669.1:g.21607263_21607264insCGGTGG	GRCh37
NC_000007.12:g.21573788_21573789insCGGTGG	NCBI36
NG_012886.2:g.29431_29432insCGGTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.1195-2424_1195-2423insCGGTGG MANE Select	ENSP00000475939.1:n.1195-2424_1195-2423in...
ENST00000328843.10:c.1195-2424_1195-2423insCGGTGG	ENSP00000330671.7:n.1195-2424_1195-2423in...
ENST00000409508.7:c.1195-2424_1195-2423insCGGTGG	ENSP00000475939.1:n.1195-2424_1195-2423in...
ENST00000496218.1:n.81-2424_81-2423insCGGTGG
ENST00000620169.4:c.1195-2424_1195-2423insCGGTGG	ENSP00000481693.1:n.1195-2424_1195-2423in...
NM_001277115.1:c.1195-2424_1195-2423insCGGTGG	NP_001264044.1:n.1195-2424_1195-2423insCG...
XR_927090.1:n.563+5680_563+5681insCCACCG
XR_001745114.1:n.2793+5680_2793+5681insCCACCG
NM_001277115.2:c.1195-2424_1195-2423insCGGTGG MANE Select	NP_001264044.1:n.1195-2424_1195-2423insCG...