Canonical Allele Identifier: CA1693557509

Gene: DNAH11

Linked Data

• dbSNP Id: rs780363860

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21567622G>C , CM000669.2:g.21567622G>C	GRCh38
NC_000007.13:g.21607240G>C , CM000669.1:g.21607240G>C	GRCh37
NC_000007.12:g.21573765G>C	NCBI36
NG_012886.2:g.29408G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.1195-2447G>C MANE Select	ENSP00000475939.1:n.1195-2447G>C
ENST00000328843.10:c.1195-2447G>C	ENSP00000330671.7:n.1195-2447G>C
ENST00000409508.7:c.1195-2447G>C	ENSP00000475939.1:n.1195-2447G>C
ENST00000496218.1:n.81-2447G>C
ENST00000620169.4:c.1195-2447G>C	ENSP00000481693.1:n.1195-2447G>C
NM_001277115.1:c.1195-2447G>C	NP_001264044.1:n.1195-2447G>C
XR_927090.1:n.563+5704C>G
XR_001745114.1:n.2793+5704C>G
NM_001277115.2:c.1195-2447G>C MANE Select	NP_001264044.1:n.1195-2447G>C