Canonical Allele Identifier: CA4181961

Gene: DNAH11

Linked Data

• ClinVar Variation Id: 226590
• ClinVar RCV Id: RCV000226484 ; RCV000222973 ; RCV003615827 ; RCV002274964
• dbSNP Id: rs72657379
• ExAC: 7:21818674 G / A
• gnomAD v2: 7-21818674-G-A
• gnomAD v3: 7-21779056-G-A
• gnomAD v4: 7-21779056-G-A
• MyVariant Identifiers: chr7:g.21818674G>A (hg19) ; chr7:g.21779056G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21779056G>A , CM000669.2:g.21779056G>A	GRCh38
NC_000007.13:g.21818674G>A , CM000669.1:g.21818674G>A	GRCh37
NC_000007.12:g.21785199G>A	NCBI36
NG_012886.2:g.240842G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.9435G>A MANE Select	ENSP00000475939.1:p.Thr3145=
ENST00000328843.10:c.9456G>A	ENSP00000330671.7:p.Thr3152=
ENST00000409508.7:c.9435G>A	ENSP00000475939.1:p.Thr3145=
ENST00000620169.4:c.9456G>A	ENSP00000481693.1:p.Thr3152=
NM_001277115.1:c.9435G>A	NP_001264044.1:p.Thr3145=
NM_001277115.2:c.9435G>A MANE Select	NP_001264044.1:p.Thr3145=