Canonical Allele Identifier: CA13350628
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs17314229

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.13974159C>T , CM000672.2:g.13974159C>T GRCh38
NC_000010.10:g.14016159C>T , CM000672.1:g.14016159C>T GRCh37
NC_000010.9:g.14056165C>T NCBI36
NG_047164.1:g.361709G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000495956.3:c.46-115247G>A ENSP00000488764.2:n.46-115247G>A
ENST00000357447.7:c.46-115247G>A MANE Select ENSP00000350032.2:n.46-115247G>A
ENST00000640906.1:c.93+33901G>A ENSP00000492091.1:n.93+33901G>A
ENST00000649423.1:c.34-115247G>A ENSP00000497182.1:n.34-115247G>A
ENST00000649947.1:c.66+50195G>A ENSP00000497500.1:n.66+50195G>A
ENST00000342409.3:n.474+33901G>A
ENST00000357447.6:c.46-115247G>A ENSP00000350032.2:n.46-115247G>A
NM_018027.3:c.46-115247G>A NP_060497.3:n.46-115247G>A
XM_005252490.2:c.93+33901G>A XP_005252547.1:n.93+33901G>A
XM_011519539.1:c.93+33901G>A XP_011517841.1:n.93+33901G>A
XM_011519543.1:c.46-115247G>A XP_011517845.1:n.46-115247G>A
XM_011519546.1:c.46-115247G>A XP_011517848.1:n.46-115247G>A
NM_001318336.1:c.93+33901G>A NP_001305265.1:n.93+33901G>A
NM_018027.4:c.46-115247G>A NP_060497.3:n.46-115247G>A
XM_005252490.3:c.93+33901G>A XP_005252547.1:n.93+33901G>A
XM_011519539.2:c.93+33901G>A XP_011517841.1:n.93+33901G>A
XM_011519543.3:c.46-115247G>A XP_011517845.1:n.46-115247G>A
XM_017016394.2:c.46-115247G>A XP_016871883.1:n.46-115247G>A
XM_017016395.2:c.34-115247G>A XP_016871884.1:n.34-115247G>A
XM_024448067.1:c.66+50195G>A XP_024303835.1:n.66+50195G>A
XM_024448068.1:c.34-115247G>A XP_024303836.1:n.34-115247G>A
XM_024448071.1:c.34-115247G>A XP_024303839.1:n.34-115247G>A
NM_018027.5:c.46-115247G>A MANE Select NP_060497.3:n.46-115247G>A
NM_001318336.2:c.93+33901G>A NP_001305265.1:n.93+33901G>A