Canonical Allele Identifier: CA1693539272
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21558875_21558876delinsAT , CM000669.2:g.21558875_21558876delinsAT GRCh38
NC_000007.13:g.21598493_21598494delinsAT , CM000669.1:g.21598493_21598494delinsAT GRCh37
NC_000007.12:g.21565018_21565019delinsAT NCBI36
NG_012886.2:g.20661_20662delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.569_570delinsAT MANE Select ENSP00000475939.1:p.Tyr190=
ENST00000328843.10:c.569_570delinsAT ENSP00000330671.7:p.Tyr190=
ENST00000409508.7:c.569_570delinsAT ENSP00000475939.1:p.Tyr190=
ENST00000620169.4:c.569_570delinsAT ENSP00000481693.1:p.Tyr190=
NM_001277115.1:c.569_570delinsAT NP_001264044.1:p.Tyr190=
NM_001277115.2:c.569_570delinsAT MANE Select NP_001264044.1:p.Tyr190=
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