Canonical Allele Identifier: CA1519938009

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284673_186284676delinsTGTG , CM000666.2:g.186284673_186284676delinsTGTG	GRCh38
NC_000004.11:g.187205827_187205830delinsTGTG , CM000666.1:g.187205827_187205830delinsTGTG	GRCh37
NC_000004.10:g.187442821_187442824delinsTGTG	NCBI36
NG_008051.1:g.23710_23713delinsTGTG , LRG_583:g.23710_23713delinsTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+413_1304+416delinsTGTG MANE Select	ENSP00000384957.2:n.1304+413_1304+416delinsTGTG
ENST00000264692.8:c.1142+413_1142+416delinsTGTG	ENSP00000264692.5:n.1142+413_1142+416delinsTGTG
ENST00000403665.6:c.1304+413_1304+416delinsTGTG	ENSP00000384957.2:n.1304+413_1304+416delinsTGTG
NM_000128.3:c.1304+413_1304+416delinsTGTG , LRG_583t1:c.1304+413_1304+416delinsTGTG	NP_000119.1:n.1304+413_1304+416delinsTGTG
XM_005262821.2:c.1307+413_1307+416delinsTGTG	XP_005262878.1:n.1307+413_1307+416delinsTGTG
XM_005262822.2:c.1307+413_1307+416delinsTGTG	XP_005262879.1:n.1307+413_1307+416delinsTGTG
XM_005262823.2:c.1037+413_1037+416delinsTGTG	XP_005262880.1:n.1037+413_1037+416delinsTGTG
XM_005262824.1:c.1307+413_1307+416delinsTGTG	XP_005262881.1:n.1307+413_1307+416delinsTGTG
XM_006714137.1:c.1259+413_1259+416delinsTGTG	XP_006714200.1:n.1259+413_1259+416delinsTGTG
XR_938706.1:n.1712+413_1712+416delinsTGTG
XR_938707.1:n.1712+413_1712+416delinsTGTG
XM_005262821.4:c.1307+413_1307+416delinsTGTG	XP_005262878.1:n.1307+413_1307+416delinsTGTG
XM_005262822.4:c.1307+413_1307+416delinsTGTG	XP_005262879.1:n.1307+413_1307+416delinsTGTG
XM_005262823.4:c.1037+413_1037+416delinsTGTG	XP_005262880.1:n.1037+413_1037+416delinsTGTG
XM_006714137.3:c.1259+413_1259+416delinsTGTG	XP_006714200.1:n.1259+413_1259+416delinsTGTG
XR_001741172.2:n.1778+413_1778+416delinsTGTG
NM_000128.4:c.1304+413_1304+416delinsTGTG MANE Select	NP_000119.1:n.1304+413_1304+416delinsTGTG