Canonical Allele Identifier: CA2838270289

Gene: FNBP1L

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.93529811_93529812insG , CM000663.2:g.93529811_93529812insG	GRCh38
NC_000001.10:g.93995368_93995369insG , CM000663.1:g.93995368_93995369insG	GRCh37
NC_000001.9:g.93767956_93767957insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271234.13:c.510+55_510+56insG MANE Select	ENSP00000271234.7:n.510+55_510+56insG
ENST00000260506.12:c.510+55_510+56insG	ENSP00000260506.8:n.510+55_510+56insG
ENST00000271234.11:c.510+55_510+56insG	ENSP00000271234.7:n.510+55_510+56insG
ENST00000370253.6:c.510+55_510+56insG	ENSP00000359275.2:n.510+55_510+56insG
ENST00000424449.2:c.47+55_47+56insG
ENST00000604705.5:c.510+55_510+56insG	ENSP00000473921.1:n.510+55_510+56insG
NM_001024948.2:c.510+55_510+56insG	NP_001020119.1:n.510+55_510+56insG
NM_001164473.2:c.510+55_510+56insG	NP_001157945.1:n.510+55_510+56insG
NM_017737.4:c.510+55_510+56insG	NP_060207.2:n.510+55_510+56insG
XM_011541625.1:c.510+55_510+56insG	XP_011539927.1:n.510+55_510+56insG
XM_011541626.1:c.234+55_234+56insG	XP_011539928.1:n.234+55_234+56insG
XM_011541625.2:c.510+55_510+56insG	XP_011539927.1:n.510+55_510+56insG
XM_017001533.1:c.234+55_234+56insG	XP_016857022.1:n.234+55_234+56insG
XR_001737248.1:n.725+55_725+56insG
NM_017737.5:c.510+55_510+56insG	NP_060207.2:n.510+55_510+56insG
NM_001024948.3:c.510+55_510+56insG	NP_001020119.1:n.510+55_510+56insG
NM_001164473.3:c.510+55_510+56insG MANE Select	NP_001157945.1:n.510+55_510+56insG