Canonical Allele Identifier: CA1099217049
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1786254095
gnomAD v3: 7-21748469-A-AGC
gnomAD v4: 7-21748469-A-AGC
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748469_21748470insGC , CM000669.2:g.21748469_21748470insGC GRCh38
NC_000007.13:g.21788087_21788088insGC , CM000669.1:g.21788087_21788088insGC GRCh37
NC_000007.12:g.21754612_21754613insGC NCBI36
NG_012886.2:g.210255_210256insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8511-111_8511-110insGC MANE Select ENSP00000475939.1:n.8511-111_8511-110insGC
ENST00000328843.10:c.8532-111_8532-110insGC ENSP00000330671.7:n.8532-111_8532-110insGC
ENST00000409508.7:c.8511-111_8511-110insGC ENSP00000475939.1:n.8511-111_8511-110insGC
ENST00000620169.4:c.8532-111_8532-110insGC ENSP00000481693.1:n.8532-111_8532-110insGC
NM_001277115.1:c.8511-111_8511-110insGC NP_001264044.1:n.8511-111_8511-110insGC
NM_001277115.2:c.8511-111_8511-110insGC MANE Select NP_001264044.1:n.8511-111_8511-110insGC
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