Canonical Allele Identifier: CA10628616
Gene: CRPPA HGNC NCBI

Linked Data

ClinVar Variation Id: 359495
ClinVar RCV Id: RCV000348239
dbSNP Id: rs886062145

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.16088426_16088434delinsC , CM000669.2:g.16088426_16088434delinsC GRCh38
NC_000007.13:g.16128051_16128059delinsC , CM000669.1:g.16128051_16128059delinsC GRCh37
NC_000007.12:g.16094576_16094584delinsC NCBI36
NG_032690.1:g.337889_337897delinsG
NG_032690.2:g.337889_337897delinsG

Transcript Alleles

HGVS Amino-acid Change
ENST00000407010.7:c.*3261_*3269delinsG MANE Select ENSP00000385478.2:n.*3261_*3269delinsG
ENST00000407010.6:c.4617_4625delinsG ENSP00000385478.2:n.4617_4625delinsG
NM_001101417.3:c.4467_4475delinsG NP_001094887.1:n.4467_4475delinsG
NM_001101426.3:c.4617_4625delinsG NP_001094896.1:n.4617_4625delinsG
XM_011515498.1:c.1251+127632_1251+127640delinsG XP_011513800.1:n.1251+127632_1251+127640delinsG
NM_001101426.4:c.*3261_*3269delinsG MANE Select NP_001094896.1:n.*3261_*3269delinsG
NM_001101417.4:c.*3261_*3269delinsG NP_001094887.1:n.*3261_*3269delinsG
NM_001368197.1:c.*3261_*3269delinsG NP_001355126.1:n.*3261_*3269delinsG
NR_160656.1:n.4682_4690delinsG