Canonical Allele Identifier: CA2458969209
Gene: FRMD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.132127858G= , CM000685.2:g.132127858G= GRCh38
NC_000023.10:g.131261886G= , CM000685.1:g.131261886G= GRCh37
NC_000023.9:g.131089567G= NCBI36
NG_012347.1:g.5165C= , LRG_867:g.5165C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298542.9:c.-14C= MANE Select ENSP00000298542.3:n.-14C=
ENST00000298542.8:c.-14C= ENSP00000298542.3:n.-14C=
NM_001306193.1:c.-14C= NP_001293122.1:n.-14C=
NM_194277.2:c.-14C= , LRG_867t1:c.-14C= NP_919253.1:n.-14C=
XM_017029948.2:c.-42C= XP_016885437.1:n.-42C=
NM_001306193.2:c.-14C= NP_001293122.1:n.-14C=
NM_194277.3:c.-14C= MANE Select NP_919253.1:n.-14C=