Canonical Allele Identifier: CA2774680428
Gene: DNAH11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21816310_21816312dup , CM000669.2:g.21816310_21816312dup GRCh38
NC_000007.13:g.21855928_21855930dup , CM000669.1:g.21855928_21855930dup GRCh37
NC_000007.12:g.21822453_21822455dup NCBI36
NG_012886.2:g.278096_278098dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.10333-157_10333-155dup MANE Select ENSP00000475939.1:n.10333-157_10333-155dup
ENST00000328843.10:c.10354-157_10354-155dup ENSP00000330671.7:n.10354-157_10354-155dup
ENST00000409508.7:c.10333-157_10333-155dup ENSP00000475939.1:n.10333-157_10333-155dup
ENST00000620169.4:c.10354-157_10354-155dup ENSP00000481693.1:n.10354-157_10354-155dup
NM_001277115.1:c.10333-157_10333-155dup NP_001264044.1:n.10333-157_10333-155dup
NM_001277115.2:c.10333-157_10333-155dup MANE Select NP_001264044.1:n.10333-157_10333-155dup