Canonical Allele Identifier: CA14159417

Gene: FRMD5

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43927409G>A , CM000677.2:g.43927409G>A	GRCh38
NC_000015.9:g.44219607G>A , CM000677.1:g.44219607G>A	GRCh37
NC_000015.8:g.42006899G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417257.6:c.103-3100C>T MANE Select	ENSP00000403067.1:n.103-3100C>T
ENST00000402883.5:c.103-3100C>T	ENSP00000384142.1:n.103-3100C>T
ENST00000417257.5:c.103-3100C>T	ENSP00000403067.1:n.103-3100C>T
ENST00000421674.5:c.103-3100C>T	ENSP00000401635.1:n.103-3100C>T
ENST00000451277.5:c.103-3100C>T	ENSP00000392786.1:n.103-3100C>T
ENST00000458630.5:c.89-3100C>T
ENST00000484674.5:c.-165-3100C>T	ENSP00000452968.1:n.-165-3100C>T
NM_001286490.1:c.-165-3100C>T	NP_001273419.1:n.-165-3100C>T
NM_001286491.1:c.-919-3100C>T	NP_001273420.1:n.-919-3100C>T
NM_032892.4:c.103-3100C>T	NP_116281.2:n.103-3100C>T
NR_104455.1:n.343-3100C>T
XM_005254730.2:c.103-3100C>T	XP_005254787.1:n.103-3100C>T
XM_011522122.1:c.103-3100C>T	XP_011520424.1:n.103-3100C>T
XM_011522123.1:c.103-3100C>T	XP_011520425.1:n.103-3100C>T
XR_931927.1:n.626-3100C>T
XR_931928.1:n.626-3100C>T
NM_001322949.1:c.103-3100C>T	NP_001309878.1:n.103-3100C>T
NM_001322950.1:c.103-3100C>T	NP_001309879.1:n.103-3100C>T
NM_001322951.1:c.103-7600C>T	NP_001309880.1:n.103-7600C>T
XM_005254730.3:c.103-3100C>T	XP_005254787.1:n.103-3100C>T
XR_931927.3:n.304-3100C>T
NM_032892.5:c.103-3100C>T MANE Select	NP_116281.2:n.103-3100C>T
NM_001286490.2:c.-165-3100C>T	NP_001273419.1:n.-165-3100C>T
NM_001286491.2:c.-919-3100C>T	NP_001273420.1:n.-919-3100C>T
NM_001322949.2:c.103-3100C>T	NP_001309878.1:n.103-3100C>T
NM_001322950.2:c.103-3100C>T	NP_001309879.1:n.103-3100C>T
NM_001322951.2:c.103-7600C>T	NP_001309880.1:n.103-7600C>T
NR_104455.2:n.320-3100C>T