Canonical Allele Identifier: CA1693605600
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21664326_21664332delinsGTTATCT , CM000669.2:g.21664326_21664332delinsGTTATCT GRCh38
NC_000007.13:g.21703944_21703950delinsGTTATCT , CM000669.1:g.21703944_21703950delinsGTTATCT GRCh37
NC_000007.12:g.21670469_21670475delinsGTTATCT NCBI36
NG_012886.2:g.126112_126118delinsGTTATCT

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.5328+5295_5328+5301delinsGTTATCT MANE Select ENSP00000475939.1:n.5328+5295_5328+5301de...
ENST00000328843.10:c.5343+5295_5343+5301delinsGTTATCT ENSP00000330671.7:n.5343+5295_5343+5301de...
ENST00000409508.7:c.5328+5295_5328+5301delinsGTTATCT ENSP00000475939.1:n.5328+5295_5328+5301de...
ENST00000620169.4:c.5343+5295_5343+5301delinsGTTATCT ENSP00000481693.1:n.5343+5295_5343+5301de...
NM_001277115.1:c.5328+5295_5328+5301delinsGTTATCT NP_001264044.1:n.5328+5295_5328+5301delin...
NM_001277115.2:c.5328+5295_5328+5301delinsGTTATCT MANE Select NP_001264044.1:n.5328+5295_5328+5301delin...
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