Canonical Allele Identifier: CA1693578921
Gene: DNAH11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21599790A= , CM000669.2:g.21599790A= GRCh38
NC_000007.13:g.21639408A= , CM000669.1:g.21639408A= GRCh37
NC_000007.12:g.21605933A= NCBI36
NG_012886.2:g.61576A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.2671A= MANE Select ENSP00000475939.1:p.Asn891=
ENST00000328843.10:c.2671A= ENSP00000330671.7:p.Asn891=
ENST00000409508.7:c.2671A= ENSP00000475939.1:p.Asn891=
ENST00000620169.4:c.2671A= ENSP00000481693.1:p.Asn891=
NM_001277115.1:c.2671A= NP_001264044.1:p.Asn891=
NM_001277115.2:c.2671A= MANE Select NP_001264044.1:p.Asn891=
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