Canonical Allele Identifier: CA227356524

Gene: WTAPP1

Linked Data

• dbSNP Id: rs768390332
• MyVariant Identifiers: chr11:g.102656434del (hg19) ; chr11:g.102785703del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102785707del , CM000673.2:g.102785707del	GRCh38
NC_000011.9:g.102656438del , CM000673.1:g.102656438del	GRCh37
NC_000011.8:g.102161648del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.325-12317del
ENST00000525739.6:n.389+1643del
ENST00000544704.1:n.344+1643del
NR_038390.1:n.389+1643del