Canonical Allele Identifier: CA2681986993
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21748493-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748493G>T , CM000669.2:g.21748493G>T GRCh38
NC_000007.13:g.21788111G>T , CM000669.1:g.21788111G>T GRCh37
NC_000007.12:g.21754636G>T NCBI36
NG_012886.2:g.210279G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8511-87G>T MANE Select ENSP00000475939.1:n.8511-87G>T
ENST00000328843.10:c.8532-87G>T ENSP00000330671.7:n.8532-87G>T
ENST00000409508.7:c.8511-87G>T ENSP00000475939.1:n.8511-87G>T
ENST00000620169.4:c.8532-87G>T ENSP00000481693.1:n.8532-87G>T
NM_001277115.1:c.8511-87G>T NP_001264044.1:n.8511-87G>T
NM_001277115.2:c.8511-87G>T MANE Select NP_001264044.1:n.8511-87G>T
Search 100 bp 5'
Search 100 bp 3'