Canonical Allele Identifier: CA2458969232
Gene: FRMD7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.132127923T= , CM000685.2:g.132127923T= GRCh38
NC_000023.10:g.131261951T= , CM000685.1:g.131261951T= GRCh37
NC_000023.9:g.131089632T= NCBI36
NG_012347.1:g.5100A= , LRG_867:g.5100A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298542.9:c.-79A= MANE Select ENSP00000298542.3:n.-79A=
ENST00000298542.8:c.-79A= ENSP00000298542.3:n.-79A=
NM_001306193.1:c.-79A= NP_001293122.1:n.-79A=
NM_194277.2:c.-79A= , LRG_867t1:c.-79A= NP_919253.1:n.-79A=
NM_001306193.2:c.-79A= NP_001293122.1:n.-79A=
NM_194277.3:c.-79A= MANE Select NP_919253.1:n.-79A=
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