Canonical Allele Identifier: CA836681100

Gene: DNAH11

Linked Data

• dbSNP Id: rs1226717098
• MyVariant Identifiers: chr7:g.21607191C>G (hg19) ; chr7:g.21567573C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21567573C>G , CM000669.2:g.21567573C>G	GRCh38
NC_000007.13:g.21607191C>G , CM000669.1:g.21607191C>G	GRCh37
NC_000007.12:g.21573716C>G	NCBI36
NG_012886.2:g.29359C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.1195-2496C>G MANE Select	ENSP00000475939.1:n.1195-2496C>G
ENST00000328843.10:c.1195-2496C>G	ENSP00000330671.7:n.1195-2496C>G
ENST00000409508.7:c.1195-2496C>G	ENSP00000475939.1:n.1195-2496C>G
ENST00000496218.1:n.81-2496C>G
ENST00000620169.4:c.1195-2496C>G	ENSP00000481693.1:n.1195-2496C>G
NM_001277115.1:c.1195-2496C>G	NP_001264044.1:n.1195-2496C>G
XR_927090.1:n.563+5753G>C
XR_001745114.1:n.2793+5753G>C
NM_001277115.2:c.1195-2496C>G MANE Select	NP_001264044.1:n.1195-2496C>G