Canonical Allele Identifier: CA227356588
Gene: WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs911316087

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102785767_102785770del , CM000673.2:g.102785767_102785770del GRCh38
NC_000011.9:g.102656498_102656501del , CM000673.1:g.102656498_102656501del GRCh37
NC_000011.8:g.102161708_102161711del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371455.7:n.325-12257_325-12254del
ENST00000525739.6:n.389+1703_389+1706del
ENST00000544704.1:n.344+1703_344+1706del
NR_038390.1:n.389+1703_389+1706del