Canonical Allele Identifier: CA155058024

Gene: DNAH11

Linked Data

• dbSNP Id: rs1045760846
• gnomAD v2: 7-21607212-A-C
• gnomAD v3: 7-21567594-A-C
• gnomAD v4: 7-21567594-A-C
• MyVariant Identifiers: chr7:g.21607212A>C (hg19) ; chr7:g.21567594A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21567594A>C , CM000669.2:g.21567594A>C	GRCh38
NC_000007.13:g.21607212A>C , CM000669.1:g.21607212A>C	GRCh37
NC_000007.12:g.21573737A>C	NCBI36
NG_012886.2:g.29380A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000409508.8:c.1195-2475A>C MANE Select	ENSP00000475939.1:n.1195-2475A>C
ENST00000328843.10:c.1195-2475A>C	ENSP00000330671.7:n.1195-2475A>C
ENST00000409508.7:c.1195-2475A>C	ENSP00000475939.1:n.1195-2475A>C
ENST00000496218.1:n.81-2475A>C
ENST00000620169.4:c.1195-2475A>C	ENSP00000481693.1:n.1195-2475A>C
NM_001277115.1:c.1195-2475A>C	NP_001264044.1:n.1195-2475A>C
XR_927090.1:n.563+5732T>G
XR_001745114.1:n.2793+5732T>G
NM_001277115.2:c.1195-2475A>C MANE Select	NP_001264044.1:n.1195-2475A>C