Canonical Allele Identifier: CA836684959
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1292310404
MyVariant Identifiers: chr7:g.21893923C>A (hg19) chr7:g.21854305C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21854305C>A , CM000669.2:g.21854305C>A GRCh38
NC_000007.13:g.21893923C>A , CM000669.1:g.21893923C>A GRCh37
NC_000007.12:g.21860448C>A NCBI36
NG_012886.2:g.316091C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11062-10C>A MANE Select ENSP00000475939.1:n.11062-10C>A
ENST00000328843.10:c.11083-10C>A ENSP00000330671.7:n.11083-10C>A
ENST00000409508.7:c.11062-10C>A ENSP00000475939.1:n.11062-10C>A
ENST00000421290.1:n.245-10C>A
ENST00000607413.5:n.325-10C>A
ENST00000620169.4:c.11083-10C>A ENSP00000481693.1:n.11083-10C>A
NM_001277115.1:c.11062-10C>A NP_001264044.1:n.11062-10C>A
NM_001277115.2:c.11062-10C>A MANE Select NP_001264044.1:n.11062-10C>A
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