Canonical Allele Identifier: CA670876366

Gene: WTAPP1

Linked Data

• dbSNP Id: rs1274105796
• MyVariant Identifiers: chr11:g.102669178_102669188del (hg19) ; chr11:g.102798447_102798457del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798449_102798459del , CM000673.2:g.102798449_102798459del	GRCh38
NC_000011.9:g.102669180_102669190del , CM000673.1:g.102669180_102669190del	GRCh37
NC_000011.8:g.102174390_102174400del	NCBI36
NG_011740.1:g.4779_4789del
NG_011740.2:g.4779_4789del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+327_423+337del
ENST00000525739.6:n.682+327_682+337del
ENST00000544704.1:n.443+327_443+337del
NR_038390.1:n.682+327_682+337del