Canonical Allele Identifier: CA453968494
Gene: DNAH11 HGNC NCBI

Linked Data

COSMIC: COSM5457322 COSM5457323
MyVariant Identifiers: chr7:g.21788261C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21748643C>T , CM000669.2:g.21748643C>T GRCh38
NC_000007.13:g.21788261C>T , CM000669.1:g.21788261C>T GRCh37
NC_000007.12:g.21754786C>T NCBI36
NG_012886.2:g.210429C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8574C>T MANE Select ENSP00000475939.1:p.Gly2858=
ENST00000328843.10:c.8595C>T ENSP00000330671.7:p.Gly2865=
ENST00000409508.7:c.8574C>T ENSP00000475939.1:p.Gly2858=
ENST00000620169.4:c.8595C>T ENSP00000481693.1:p.Gly2865=
NM_001277115.1:c.8574C>T NP_001264044.1:p.Gly2858=
NM_001277115.2:c.8574C>T MANE Select NP_001264044.1:p.Gly2858=
Search 100 bp 5'
Search 100 bp 3'