Canonical Allele Identifier: CA366949325

Gene: DNAH11

Linked Data

• MyVariant Identifiers: chr7:g.21856322T>A (hg19) ; chr7:g.21816704T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21816704T>A , CM000669.2:g.21816704T>A	GRCh38
NC_000007.13:g.21856322T>A , CM000669.1:g.21856322T>A	GRCh37
NC_000007.12:g.21822847T>A	NCBI36
NG_012886.2:g.278490T>A

Transcript Alleles

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