Canonical Allele Identifier: CA1693571387
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619061_21619063delinsATG , CM000669.2:g.21619061_21619063delinsATG GRCh38
NC_000007.13:g.21658679_21658681delinsATG , CM000669.1:g.21658679_21658681delinsATG GRCh37
NC_000007.12:g.21625204_21625206delinsATG NCBI36
NG_012886.2:g.80847_80849delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4255-39_4255-37delinsATG MANE Select ENSP00000475939.1:n.4255-39_4255-37delinsATG
ENST00000328843.10:c.4270-39_4270-37delinsATG ENSP00000330671.7:n.4270-39_4270-37delinsATG
ENST00000409508.7:c.4255-39_4255-37delinsATG ENSP00000475939.1:n.4255-39_4255-37delinsATG
ENST00000465593.1:n.281-39_281-37delinsATG
ENST00000620169.4:c.4270-39_4270-37delinsATG ENSP00000481693.1:n.4270-39_4270-37delinsATG
NM_001277115.1:c.4255-39_4255-37delinsATG NP_001264044.1:n.4255-39_4255-37delinsATG
NM_001277115.2:c.4255-39_4255-37delinsATG MANE Select NP_001264044.1:n.4255-39_4255-37delinsATG