Canonical Allele Identifier: CA2713980662

Gene: DNAH11

Linked Data

• dbSNP Id: rs2127999990

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816262_21816268del , CM000669.2:g.21816262_21816268del	GRCh38
NC_000007.13:g.21855880_21855886del , CM000669.1:g.21855880_21855886del	GRCh37
NC_000007.12:g.21822405_21822411del	NCBI36
NG_012886.2:g.278048_278054del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10333-205_10333-199del MANE Select	ENSP00000475939.1:n.10333-205_10333-199del
ENST00000328843.10:c.10354-205_10354-199del	ENSP00000330671.7:n.10354-205_10354-199del
ENST00000409508.7:c.10333-205_10333-199del	ENSP00000475939.1:n.10333-205_10333-199del
ENST00000620169.4:c.10354-205_10354-199del	ENSP00000481693.1:n.10354-205_10354-199del
NM_001277115.1:c.10333-205_10333-199del	NP_001264044.1:n.10333-205_10333-199del
NM_001277115.2:c.10333-205_10333-199del MANE Select	NP_001264044.1:n.10333-205_10333-199del