Canonical Allele Identifier: CA917960908
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1583534739

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21619206_21619207insATCTTAACTAAAATATACTCAAGTCAGGT , CM000669.2:g.21619206_21619207insATCTTAACTAAAATATACTCAAGTCAGGT GRCh38
NC_000007.13:g.21658824_21658825insATCTTAACTAAAATATACTCAAGTCAGGT , CM000669.1:g.21658824_21658825insATCTTAACTAAAATATACTCAAGTCAGGT GRCh37
NC_000007.12:g.21625349_21625350insATCTTAACTAAAATATACTCAAGTCAGGT NCBI36
NG_012886.2:g.80992_80993insATCTTAACTAAAATATACTCAAGTCAGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.4361_4362insATCTTAACTAAAATATACTCAAGTCAGGT MANE Select ENSP00000475939.1:p.Leu1455SerfsTer2
ENST00000328843.10:c.4376_4377insATCTTAACTAAAATATACTCAAGTCAGGT ENSP00000330671.7:p.Leu1460SerfsTer2
ENST00000409508.7:c.4361_4362insATCTTAACTAAAATATACTCAAGTCAGGT ENSP00000475939.1:p.Leu1455SerfsTer2
ENST00000465593.1:n.387_388insATCTTAACTAAAATATACTCAAGTCAGGT
ENST00000620169.4:c.4376_4377insATCTTAACTAAAATATACTCAAGTCAGGT ENSP00000481693.1:p.Leu1460SerfsTer2
NM_001277115.1:c.4361_4362insATCTTAACTAAAATATACTCAAGTCAGGT NP_001264044.1:p.Leu1455SerfsTer2
NM_001277115.2:c.4361_4362insATCTTAACTAAAATATACTCAAGTCAGGT MANE Select NP_001264044.1:p.Leu1455SerfsTer2