Canonical Allele Identifier: CA155121947

Gene: DNAH11

Linked Data

• dbSNP Id: rs977417389
• MyVariant Identifiers: chr7:g.21855901A>C (hg19) ; chr7:g.21816283A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816283A>C , CM000669.2:g.21816283A>C	GRCh38
NC_000007.13:g.21855901A>C , CM000669.1:g.21855901A>C	GRCh37
NC_000007.12:g.21822426A>C	NCBI36
NG_012886.2:g.278069A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.10333-184A>C MANE Select	ENSP00000475939.1:n.10333-184A>C
ENST00000328843.10:c.10354-184A>C	ENSP00000330671.7:n.10354-184A>C
ENST00000409508.7:c.10333-184A>C	ENSP00000475939.1:n.10333-184A>C
ENST00000620169.4:c.10354-184A>C	ENSP00000481693.1:n.10354-184A>C
NM_001277115.1:c.10333-184A>C	NP_001264044.1:n.10333-184A>C
NM_001277115.2:c.10333-184A>C MANE Select	NP_001264044.1:n.10333-184A>C