Canonical Allele Identifier: CA2458969217
Gene: FRMD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.132127882T= , CM000685.2:g.132127882T= GRCh38
NC_000023.10:g.131261910T= , CM000685.1:g.131261910T= GRCh37
NC_000023.9:g.131089591T= NCBI36
NG_012347.1:g.5141A= , LRG_867:g.5141A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298542.9:c.-38A= MANE Select ENSP00000298542.3:n.-38A=
ENST00000298542.8:c.-38A= ENSP00000298542.3:n.-38A=
NM_001306193.1:c.-38A= NP_001293122.1:n.-38A=
NM_194277.2:c.-38A= , LRG_867t1:c.-38A= NP_919253.1:n.-38A=
XM_017029948.2:c.-66A= XP_016885437.1:n.-66A=
NM_001306193.2:c.-38A= NP_001293122.1:n.-38A=
NM_194277.3:c.-38A= MANE Select NP_919253.1:n.-38A=