Canonical Allele Identifier: CA1693539712

Gene: DNAH11

Linked Data

• dbSNP Id: rs1203566996
• gnomAD v4: 7-21559014-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21559014A>C , CM000669.2:g.21559014A>C	GRCh38
NC_000007.13:g.21598632A>C , CM000669.1:g.21598632A>C	GRCh37
NC_000007.12:g.21565157A>C	NCBI36
NG_012886.2:g.20800A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.692+16A>C MANE Select	ENSP00000475939.1:n.692+16A>C
ENST00000328843.10:c.692+16A>C	ENSP00000330671.7:n.692+16A>C
ENST00000409508.7:c.692+16A>C	ENSP00000475939.1:n.692+16A>C
ENST00000620169.4:c.692+16A>C	ENSP00000481693.1:n.692+16A>C
NM_001277115.1:c.692+16A>C	NP_001264044.1:n.692+16A>C
NM_001277115.2:c.692+16A>C MANE Select	NP_001264044.1:n.692+16A>C