Canonical Allele Identifier: CA2838351122
Gene: FRMD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44116237_44116242dup , CM000677.2:g.44116237_44116242dup GRCh38
NC_000015.9:g.44408435_44408440dup , CM000677.1:g.44408435_44408440dup GRCh37
NC_000015.8:g.42195727_42195732dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000417257.6:c.102+78721_102+78726dup MANE Select ENSP00000403067.1:n.102+78721_102+78726dup
ENST00000402883.5:c.102+78721_102+78726dup ENSP00000384142.1:n.102+78721_102+78726dup
ENST00000417257.5:c.102+78721_102+78726dup ENSP00000403067.1:n.102+78721_102+78726dup
ENST00000421674.5:c.102+78721_102+78726dup ENSP00000401635.1:n.102+78721_102+78726dup
ENST00000451277.5:c.102+78721_102+78726dup ENSP00000392786.1:n.102+78721_102+78726dup
ENST00000458630.5:c.88+78721_88+78726dup
ENST00000484674.5:c.-237-14702_-237-14697dup ENSP00000452968.1:n.-237-14702_-237-14697dup
NM_001286490.1:c.-237-14702_-237-14697dup NP_001273419.1:n.-237-14702_-237-14697dup
NM_001286491.1:c.-920+78721_-920+78726dup NP_001273420.1:n.-920+78721_-920+78726dup
NM_032892.4:c.102+78721_102+78726dup NP_116281.2:n.102+78721_102+78726dup
NR_104455.1:n.342+78721_342+78726dup
XM_005254730.2:c.102+78721_102+78726dup XP_005254787.1:n.102+78721_102+78726dup
XM_011522122.1:c.102+78721_102+78726dup XP_011520424.1:n.102+78721_102+78726dup
XM_011522123.1:c.102+78721_102+78726dup XP_011520425.1:n.102+78721_102+78726dup
XR_931927.1:n.625+78721_625+78726dup
XR_931928.1:n.625+78721_625+78726dup
NM_001322949.1:c.102+78721_102+78726dup NP_001309878.1:n.102+78721_102+78726dup
NM_001322950.1:c.102+78721_102+78726dup NP_001309879.1:n.102+78721_102+78726dup
NM_001322951.1:c.102+78721_102+78726dup NP_001309880.1:n.102+78721_102+78726dup
XM_005254730.3:c.102+78721_102+78726dup XP_005254787.1:n.102+78721_102+78726dup
XR_931927.3:n.303+78721_303+78726dup
NM_032892.5:c.102+78721_102+78726dup MANE Select NP_116281.2:n.102+78721_102+78726dup
NM_001286490.2:c.-237-14702_-237-14697dup NP_001273419.1:n.-237-14702_-237-14697dup
NM_001286491.2:c.-920+78721_-920+78726dup NP_001273420.1:n.-920+78721_-920+78726dup
NM_001322949.2:c.102+78721_102+78726dup NP_001309878.1:n.102+78721_102+78726dup
NM_001322950.2:c.102+78721_102+78726dup NP_001309879.1:n.102+78721_102+78726dup
NM_001322951.2:c.102+78721_102+78726dup NP_001309880.1:n.102+78721_102+78726dup
NR_104455.2:n.319+78721_319+78726dup