Canonical Allele Identifier: CA2458969249
Gene: FRMD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.132127946C= , CM000685.2:g.132127946C= GRCh38
NC_000023.10:g.131261974C= , CM000685.1:g.131261974C= GRCh37
NC_000023.9:g.131089655C= NCBI36
NG_012347.1:g.5077G= , LRG_867:g.5077G=

Transcript Alleles

HGVS Amino-acid change
ENST00000298542.9:c.-102G= MANE Select ENSP00000298542.3:n.-102G=
ENST00000298542.8:c.-102G= ENSP00000298542.3:n.-102G=
NM_001306193.1:c.-102G= NP_001293122.1:n.-102G=
NM_194277.2:c.-102G= , LRG_867t1:c.-102G= NP_919253.1:n.-102G=
NM_001306193.2:c.-102G= NP_001293122.1:n.-102G=
NM_194277.3:c.-102G= MANE Select NP_919253.1:n.-102G=