Canonical Allele Identifier: CA2458969253
Gene: FRMD7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.132127951A= , CM000685.2:g.132127951A= GRCh38
NC_000023.10:g.131261979A= , CM000685.1:g.131261979A= GRCh37
NC_000023.9:g.131089660A= NCBI36
NG_012347.1:g.5072T= , LRG_867:g.5072T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298542.9:c.-107T= MANE Select ENSP00000298542.3:n.-107T=
ENST00000298542.8:c.-107T= ENSP00000298542.3:n.-107T=
NM_001306193.1:c.-107T= NP_001293122.1:n.-107T=
NM_194277.2:c.-107T= , LRG_867t1:c.-107T= NP_919253.1:n.-107T=
NM_001306193.2:c.-107T= NP_001293122.1:n.-107T=
NM_194277.3:c.-107T= MANE Select NP_919253.1:n.-107T=
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