Canonical Allele Identifier: CA1693538808

Gene: DNAH11

Linked Data

• dbSNP Id: rs1583479734

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21558627T>C , CM000669.2:g.21558627T>C	GRCh38
NC_000007.13:g.21598245T>C , CM000669.1:g.21598245T>C	GRCh37
NC_000007.12:g.21564770T>C	NCBI36
NG_012886.2:g.20413T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.496-175T>C MANE Select	ENSP00000475939.1:n.496-175T>C
ENST00000328843.10:c.496-175T>C	ENSP00000330671.7:n.496-175T>C
ENST00000409508.7:c.496-175T>C	ENSP00000475939.1:n.496-175T>C
ENST00000620169.4:c.496-175T>C	ENSP00000481693.1:n.496-175T>C
NM_001277115.1:c.496-175T>C	NP_001264044.1:n.496-175T>C
NM_001277115.2:c.496-175T>C MANE Select	NP_001264044.1:n.496-175T>C