Canonical Allele Identifier: CA366964239
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21920505C>A (hg19) chr7:g.21880887C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880887C>A , CM000669.2:g.21880887C>A GRCh38
NC_000007.13:g.21920505C>A , CM000669.1:g.21920505C>A GRCh37
NC_000007.12:g.21887030C>A NCBI36
NG_012886.2:g.342673C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12381C>A MANE Select ENSP00000475939.1:p.Asn4127Lys
ENST00000328843.10:c.12402C>A ENSP00000330671.7:p.Asn4134Lys
ENST00000409508.7:c.12381C>A ENSP00000475939.1:p.Asn4127Lys
ENST00000620169.4:c.12402C>A ENSP00000481693.1:p.Asn4134Lys
NM_001277115.1:c.12381C>A NP_001264044.1:p.Asn4127Lys
NM_001277115.2:c.12381C>A MANE Select NP_001264044.1:p.Asn4127Lys
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