Canonical Allele Identifier: CA366931138
Gene: DNAH11 HGNC NCBI

Linked Data

gnomAD v4: 7-21543347-G-C
MyVariant Identifiers: chr7:g.21582965G>C (hg19) chr7:g.21543347G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21543347G>C , CM000669.2:g.21543347G>C GRCh38
NC_000007.13:g.21582965G>C , CM000669.1:g.21582965G>C GRCh37
NC_000007.12:g.21549490G>C NCBI36
NG_012886.2:g.5133G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.102G>C MANE Select ENSP00000475939.1:p.Glu34Asp
ENST00000328843.10:c.102G>C ENSP00000330671.7:p.Glu34Asp
ENST00000409508.7:c.102G>C ENSP00000475939.1:p.Glu34Asp
ENST00000620169.4:c.102G>C ENSP00000481693.1:p.Glu34Asp
NM_001277115.1:c.102G>C NP_001264044.1:p.Glu34Asp
NM_001277115.2:c.102G>C MANE Select NP_001264044.1:p.Glu34Asp
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