Canonical Allele Identifier: CA1693605584
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21664298_21664299delinsAT , CM000669.2:g.21664298_21664299delinsAT GRCh38
NC_000007.13:g.21703916_21703917delinsAT , CM000669.1:g.21703916_21703917delinsAT GRCh37
NC_000007.12:g.21670441_21670442delinsAT NCBI36
NG_012886.2:g.126084_126085delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.5328+5267_5328+5268delinsAT MANE Select ENSP00000475939.1:n.5328+5267_5328+5268de...
ENST00000328843.10:c.5343+5267_5343+5268delinsAT ENSP00000330671.7:n.5343+5267_5343+5268de...
ENST00000409508.7:c.5328+5267_5328+5268delinsAT ENSP00000475939.1:n.5328+5267_5328+5268de...
ENST00000620169.4:c.5343+5267_5343+5268delinsAT ENSP00000481693.1:n.5343+5267_5343+5268de...
NM_001277115.1:c.5328+5267_5328+5268delinsAT NP_001264044.1:n.5328+5267_5328+5268delin...
NM_001277115.2:c.5328+5267_5328+5268delinsAT MANE Select NP_001264044.1:n.5328+5267_5328+5268delin...