Canonical Allele Identifier: CA601246163

Gene: WTAPP1

Linked Data

• dbSNP Id: rs1231661140
• gnomAD v2: 11-102669179-CAA-C
• gnomAD v3: 11-102798448-CAA-C
• gnomAD v4: 11-102798448-CAA-C
• MyVariant Identifiers: chr11:g.102669180_102669181del (hg19) ; chr11:g.102798449_102798450del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798450_102798451del , CM000673.2:g.102798450_102798451del	GRCh38
NC_000011.9:g.102669181_102669182del , CM000673.1:g.102669181_102669182del	GRCh37
NC_000011.8:g.102174391_102174392del	NCBI36
NG_011740.1:g.4786_4787del
NG_011740.2:g.4786_4787del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+328_423+329del
ENST00000525739.6:n.682+328_682+329del
ENST00000544704.1:n.443+328_443+329del
NR_038390.1:n.682+328_682+329del