Canonical Allele Identifier: CA2458969256
Gene: FRMD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.132127971A= , CM000685.2:g.132127971A= GRCh38
NC_000023.10:g.131261999A= , CM000685.1:g.131261999A= GRCh37
NC_000023.9:g.131089680A= NCBI36
NG_012347.1:g.5052T= , LRG_867:g.5052T=

Transcript Alleles

HGVS Amino-acid change
ENST00000298542.9:c.-127T= MANE Select ENSP00000298542.3:n.-127T=
ENST00000298542.8:c.-127T= ENSP00000298542.3:n.-127T=
NM_001306193.1:c.-127T= NP_001293122.1:n.-127T=
NM_194277.2:c.-127T= , LRG_867t1:c.-127T= NP_919253.1:n.-127T=
NM_001306193.2:c.-127T= NP_001293122.1:n.-127T=
NM_194277.3:c.-127T= MANE Select NP_919253.1:n.-127T=