Canonical Allele Identifier: CA2838419024

Gene: FNBP4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47767025_47767027del , CM000673.2:g.47767025_47767027del	GRCh38
NC_000011.9:g.47788577_47788579del , CM000673.1:g.47788577_47788579del	GRCh37
NC_000011.8:g.47745153_47745155del	NCBI36
NG_053146.1:g.5454_5456del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263773.10:c.220+44_220+46del MANE Select	ENSP00000263773.5:n.220+44_220+46del
ENST00000263773.9:c.220+44_220+46del	ENSP00000263773.5:n.220+44_220+46del
ENST00000534003.5:n.218+44_218+46del
ENST00000540172.2:c.220+44_220+46del	ENSP00000440181.2:n.220+44_220+46del
ENST00000542975.1:n.375+44_375+46del
NM_015308.2:c.220+44_220+46del	NP_056123.2:n.220+44_220+46del
XM_005252833.2:c.226+38_226+40del	XP_005252890.1:n.226+38_226+40del
XM_005252834.2:c.226+38_226+40del	XP_005252891.1:n.226+38_226+40del
XM_006718171.1:c.226+38_226+40del	XP_006718234.1:n.226+38_226+40del
XM_011519954.1:c.226+38_226+40del	XP_011518256.1:n.226+38_226+40del
XR_242785.1:n.398+38_398+40del
XR_242786.1:n.398+38_398+40del
XR_930854.1:n.398+38_398+40del
XR_930855.1:n.398+38_398+40del
XR_930856.1:n.398+38_398+40del
XR_930857.1:n.398+38_398+40del
NM_001318339.2:c.226+38_226+40del	NP_001305268.1:n.226+38_226+40del
NM_015308.4:c.220+44_220+46del	NP_056123.2:n.220+44_220+46del
XM_024448408.1:c.226+38_226+40del	XP_024304176.1:n.226+38_226+40del
XM_024448409.1:c.226+38_226+40del	XP_024304177.1:n.226+38_226+40del
XR_001747804.1:n.398+38_398+40del
XR_001747810.1:n.398+38_398+40del
XR_001747813.1:n.385+44_385+46del
XR_001747815.1:n.385+44_385+46del
XR_002957134.1:n.398+38_398+40del
XR_002957135.1:n.385+44_385+46del
XR_002957136.1:n.398+38_398+40del
XR_242785.2:n.398+38_398+40del
XR_930855.2:n.398+38_398+40del
NM_001318339.3:c.226+38_226+40del	NP_001305268.1:n.226+38_226+40del
NM_015308.5:c.220+44_220+46del MANE Select	NP_056123.2:n.220+44_220+46del