Canonical Allele Identifier: CA1519931297

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186271102_186271103delinsTG , CM000666.2:g.186271102_186271103delinsTG	GRCh38
NC_000004.11:g.187192256_187192257delinsTG , CM000666.1:g.187192256_187192257delinsTG	GRCh37
NC_000004.10:g.187429250_187429251delinsTG	NCBI36
NG_008051.1:g.10139_10140delinsTG , LRG_583:g.10139_10140delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.56-507_56-506delinsTG MANE Select	ENSP00000384957.2:n.56-507_56-506delinsTG
ENST00000264692.8:c.56-507_56-506delinsTG	ENSP00000264692.5:n.56-507_56-506delinsTG
ENST00000403665.6:c.56-507_56-506delinsTG	ENSP00000384957.2:n.56-507_56-506delinsTG
ENST00000492972.6:c.56-507_56-506delinsTG	ENSP00000424479.1:n.56-507_56-506delinsTG
NM_000128.3:c.56-507_56-506delinsTG , LRG_583t1:c.56-507_56-506delinsTG	NP_000119.1:n.56-507_56-506delinsTG
XM_005262821.2:c.56-507_56-506delinsTG	XP_005262878.1:n.56-507_56-506delinsTG
XM_005262822.2:c.56-507_56-506delinsTG	XP_005262879.1:n.56-507_56-506delinsTG
XM_005262823.2:c.56-507_56-506delinsTG	XP_005262880.1:n.56-507_56-506delinsTG
XM_005262824.1:c.56-507_56-506delinsTG	XP_005262881.1:n.56-507_56-506delinsTG
XM_006714137.1:c.56-507_56-506delinsTG	XP_006714200.1:n.56-507_56-506delinsTG
XR_938706.1:n.408-507_408-506delinsTG
XR_938707.1:n.408-507_408-506delinsTG
NM_001354804.1:c.56-507_56-506delinsTG	NP_001341733.1:n.56-507_56-506delinsTG
XM_005262821.4:c.56-507_56-506delinsTG	XP_005262878.1:n.56-507_56-506delinsTG
XM_005262822.4:c.56-507_56-506delinsTG	XP_005262879.1:n.56-507_56-506delinsTG
XM_005262823.4:c.56-507_56-506delinsTG	XP_005262880.1:n.56-507_56-506delinsTG
XM_006714137.3:c.56-507_56-506delinsTG	XP_006714200.1:n.56-507_56-506delinsTG
XM_017007884.2:c.56-507_56-506delinsTG	XP_016863373.1:n.56-507_56-506delinsTG
XM_017007885.2:c.56-507_56-506delinsTG	XP_016863374.1:n.56-507_56-506delinsTG
XM_017007886.2:c.56-507_56-506delinsTG	XP_016863375.1:n.56-507_56-506delinsTG
XR_001741172.2:n.389-507_389-506delinsTG
NM_000128.4:c.56-507_56-506delinsTG MANE Select	NP_000119.1:n.56-507_56-506delinsTG
NM_001354804.2:c.56-507_56-506delinsTG	NP_001341733.1:n.56-507_56-506delinsTG