Canonical Allele Identifier: CA1099217036
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1786253744
gnomAD v3: 7-21748466-GCA-G
gnomAD v4: 7-21748466-GCA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748467_21748468del , CM000669.2:g.21748467_21748468del GRCh38
NC_000007.13:g.21788085_21788086del , CM000669.1:g.21788085_21788086del GRCh37
NC_000007.12:g.21754610_21754611del NCBI36
NG_012886.2:g.210253_210254del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8511-113_8511-112del MANE Select ENSP00000475939.1:n.8511-113_8511-112del
ENST00000328843.10:c.8532-113_8532-112del ENSP00000330671.7:n.8532-113_8532-112del
ENST00000409508.7:c.8511-113_8511-112del ENSP00000475939.1:n.8511-113_8511-112del
ENST00000620169.4:c.8532-113_8532-112del ENSP00000481693.1:n.8532-113_8532-112del
NM_001277115.1:c.8511-113_8511-112del NP_001264044.1:n.8511-113_8511-112del
NM_001277115.2:c.8511-113_8511-112del MANE Select NP_001264044.1:n.8511-113_8511-112del
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