Canonical Allele Identifier: CA366961642
Gene: DNAH11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.21904194T>G (hg19) chr7:g.21864576T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21864576T>G , CM000669.2:g.21864576T>G GRCh38
NC_000007.13:g.21904194T>G , CM000669.1:g.21904194T>G GRCh37
NC_000007.12:g.21870719T>G NCBI36
NG_012886.2:g.326362T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.11415T>G MANE Select ENSP00000475939.1:p.Asp3805Glu
ENST00000328843.10:c.11436T>G ENSP00000330671.7:p.Asp3812Glu
ENST00000409508.7:c.11415T>G ENSP00000475939.1:p.Asp3805Glu
ENST00000620169.4:c.11436T>G ENSP00000481693.1:p.Asp3812Glu
NM_001277115.1:c.11415T>G NP_001264044.1:p.Asp3805Glu
NM_001277115.2:c.11415T>G MANE Select NP_001264044.1:p.Asp3805Glu
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