Canonical Allele Identifier: CA2681984299

Gene: DNAH11

Linked Data

• gnomAD v4: 7-21705439-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21705439A>C , CM000669.2:g.21705439A>C	GRCh38
NC_000007.13:g.21745057A>C , CM000669.1:g.21745057A>C	GRCh37
NC_000007.12:g.21711582A>C	NCBI36
NG_012886.2:g.167225A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.6469-21A>C MANE Select	ENSP00000475939.1:n.6469-21A>C
ENST00000328843.10:c.6490-21A>C	ENSP00000330671.7:n.6490-21A>C
ENST00000409508.7:c.6469-21A>C	ENSP00000475939.1:n.6469-21A>C
ENST00000620169.4:c.6490-21A>C	ENSP00000481693.1:n.6490-21A>C
NM_001277115.1:c.6469-21A>C	NP_001264044.1:n.6469-21A>C
NM_001277115.2:c.6469-21A>C MANE Select	NP_001264044.1:n.6469-21A>C