Canonical Allele Identifier: CA917960699
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs1562666443

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21567543_21567544del , CM000669.2:g.21567543_21567544del GRCh38
NC_000007.13:g.21607161_21607162del , CM000669.1:g.21607161_21607162del GRCh37
NC_000007.12:g.21573686_21573687del NCBI36
NG_012886.2:g.29329_29330del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.1195-2526_1195-2525del MANE Select ENSP00000475939.1:n.1195-2526_1195-2525del
ENST00000328843.10:c.1195-2526_1195-2525del ENSP00000330671.7:n.1195-2526_1195-2525del
ENST00000409508.7:c.1195-2526_1195-2525del ENSP00000475939.1:n.1195-2526_1195-2525del
ENST00000496218.1:n.81-2526_81-2525del
ENST00000620169.4:c.1195-2526_1195-2525del ENSP00000481693.1:n.1195-2526_1195-2525del
NM_001277115.1:c.1195-2526_1195-2525del NP_001264044.1:n.1195-2526_1195-2525del
XR_927090.1:n.563+5785_563+5786del
XR_001745114.1:n.2793+5785_2793+5786del
NM_001277115.2:c.1195-2526_1195-2525del MANE Select NP_001264044.1:n.1195-2526_1195-2525del