Canonical Allele Identifier: CA1693666665

Gene: DNAH11

Linked Data

• dbSNP Id: rs1789815527
• gnomAD v4: 7-21816785-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816785G>C , CM000669.2:g.21816785G>C	GRCh38
NC_000007.13:g.21856403G>C , CM000669.1:g.21856403G>C	GRCh37
NC_000007.12:g.21822928G>C	NCBI36
NG_012886.2:g.278571G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10568+83G>C MANE Select	ENSP00000475939.1:n.10568+83G>C
ENST00000328843.10:c.10589+83G>C	ENSP00000330671.7:n.10589+83G>C
ENST00000409508.7:c.10568+83G>C	ENSP00000475939.1:n.10568+83G>C
ENST00000620169.4:c.10589+83G>C	ENSP00000481693.1:n.10589+83G>C
NM_001277115.1:c.10568+83G>C	NP_001264044.1:n.10568+83G>C
NM_001277115.2:c.10568+83G>C MANE Select	NP_001264044.1:n.10568+83G>C