Canonical Allele Identifier: CA2581034706
Gene: WTAPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102799093A= , CM000673.2:g.102799093A= GRCh38
NC_000011.9:g.102669824A= , CM000673.1:g.102669824A= GRCh37
NC_000011.8:g.102175034A= NCBI36
NG_011740.1:g.4143T=
NG_011740.2:g.4143T=

Transcript Alleles

HGVS Amino-acid Change
NR_038390.1:n.682+971A=
ENST00000371455.7:n.423+971A=
ENST00000525739.6:n.682+971A=
ENST00000544704.1:n.443+971A=