Canonical Allele Identifier: CA836681124

Gene: DNAH11

Linked Data

• dbSNP Id: rs1320145166
• MyVariant Identifiers: chr7:g.21607278_21607279del (hg19) ; chr7:g.21567660_21567661del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21567660_21567661del , CM000669.2:g.21567660_21567661del	GRCh38
NC_000007.13:g.21607278_21607279del , CM000669.1:g.21607278_21607279del	GRCh37
NC_000007.12:g.21573803_21573804del	NCBI36
NG_012886.2:g.29446_29447del

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.1195-2409_1195-2408del MANE Select	ENSP00000475939.1:n.1195-2409_1195-2408de...
ENST00000328843.10:c.1195-2409_1195-2408del	ENSP00000330671.7:n.1195-2409_1195-2408de...
ENST00000409508.7:c.1195-2409_1195-2408del	ENSP00000475939.1:n.1195-2409_1195-2408de...
ENST00000496218.1:n.81-2409_81-2408del
ENST00000620169.4:c.1195-2409_1195-2408del	ENSP00000481693.1:n.1195-2409_1195-2408de...
NM_001277115.1:c.1195-2409_1195-2408del	NP_001264044.1:n.1195-2409_1195-2408del
XR_927090.1:n.563+5665_563+5666del
XR_001745114.1:n.2793+5665_2793+5666del
NM_001277115.2:c.1195-2409_1195-2408del MANE Select	NP_001264044.1:n.1195-2409_1195-2408del