Canonical Allele Identifier: CA155122451
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1041438557
gnomAD v3: 7-21816988-T-TA
gnomAD v4: 7-21816988-T-TA
MyVariant Identifiers: chr7:g.21856606_21856607insA (hg19) chr7:g.21816988_21816989insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816989dup , CM000669.2:g.21816989dup GRCh38
NC_000007.13:g.21856607dup , CM000669.1:g.21856607dup GRCh37
NC_000007.12:g.21823132dup NCBI36
NG_012886.2:g.278775dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10568+287dup MANE Select ENSP00000475939.1:n.10568+287dup
ENST00000328843.10:c.10589+287dup ENSP00000330671.7:n.10589+287dup
ENST00000409508.7:c.10568+287dup ENSP00000475939.1:n.10568+287dup
ENST00000620169.4:c.10589+287dup ENSP00000481693.1:n.10589+287dup
NM_001277115.1:c.10568+287dup NP_001264044.1:n.10568+287dup
NM_001277115.2:c.10568+287dup MANE Select NP_001264044.1:n.10568+287dup
Search 100 bp 5'
Search 100 bp 3'