Canonical Allele Identifier: CA4179433

Gene: DNAH11

Linked Data

• ClinVar Variation Id: 257879
• ClinVar RCV Id: RCV000459210 ; RCV001567623 ; RCV004529427
• dbSNP Id: rs201386161
• ExAC: 7:21639520 A / T
• gnomAD v2: 7-21639520-A-T
• gnomAD v3: 7-21599902-A-T
• gnomAD v4: 7-21599902-A-T
• MyVariant Identifiers: chr7:g.21639520A>T (hg19) ; chr7:g.21599902A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.21599902A>T , CM000669.2:g.21599902A>T	GRCh38
NC_000007.13:g.21639520A>T , CM000669.1:g.21639520A>T	GRCh37
NC_000007.12:g.21606045A>T	NCBI36
NG_012886.2:g.61688A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409508.8:c.2783A>T MANE Select	ENSP00000475939.1:p.Asp928Val
ENST00000328843.10:c.2783A>T	ENSP00000330671.7:p.Asp928Val
ENST00000409508.7:c.2783A>T	ENSP00000475939.1:p.Asp928Val
ENST00000620169.4:c.2783A>T	ENSP00000481693.1:p.Asp928Val
NM_001277115.1:c.2783A>T	NP_001264044.1:p.Asp928Val
NM_001277115.2:c.2783A>T MANE Select	NP_001264044.1:p.Asp928Val