Canonical Allele Identifier: CA1693663152
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21749707T= , CM000669.2:g.21749707T= GRCh38
NC_000007.13:g.21789325T= , CM000669.1:g.21789325T= GRCh37
NC_000007.12:g.21755850T= NCBI36
NG_012886.2:g.211493T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.8703T= MANE Select ENSP00000475939.1:p.Thr2901=
ENST00000328843.10:c.8724T= ENSP00000330671.7:p.Thr2908=
ENST00000409508.7:c.8703T= ENSP00000475939.1:p.Thr2901=
ENST00000620169.4:c.8724T= ENSP00000481693.1:p.Thr2908=
NM_001277115.1:c.8703T= NP_001264044.1:p.Thr2901=
NM_001277115.2:c.8703T= MANE Select NP_001264044.1:p.Thr2901=
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