Canonical Allele Identifier: CA10636488
Gene: ANKRD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 301594
ClinVar RCV Id: RCV000276837
dbSNP Id: rs71025330
gnomAD v3: 10-90912291-T-TAAAA
gnomAD v4: 10-90912291-T-TAAAA
MyVariant Identifiers: chr10:g.92672049_92672052dupAAAA (hg19) chr10:g.92672048_92672049insAAAA (hg19) chr10:g.90912292_90912295dupAAAA (hg38) chr10:g.90912291_90912292insAAAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.90912318_90912321dup , CM000672.2:g.90912318_90912321dup GRCh38
NC_000010.10:g.92672075_92672078dup , CM000672.1:g.92672075_92672078dup GRCh37
NC_000010.9:g.92662055_92662058dup NCBI36
NG_023227.1:g.13981_13984dup , LRG_379:g.13981_13984dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371697.4:c.*571_*574dup MANE Select ENSP00000360762.3:n.*571_*574dup
ENST00000371697.3:c.*571_*574dup ENSP00000360762.3:n.*571_*574dup
NM_014391.2:c.*571_*574dup , LRG_379t1:c.*571_*574dup NP_055206.2:n.*571_*574dup
NM_014391.3:c.*571_*574dup MANE Select NP_055206.2:n.*571_*574dup
Search 100 bp 5'
Search 100 bp 3'