Canonical Allele Identifier: CA1519937727

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284084_186284088delinsTGTTG , CM000666.2:g.186284084_186284088delinsTGTTG	GRCh38
NC_000004.11:g.187205238_187205242delinsTGTTG , CM000666.1:g.187205238_187205242delinsTGTTG	GRCh37
NC_000004.10:g.187442232_187442236delinsTGTTG	NCBI36
NG_008051.1:g.23121_23125delinsTGTTG , LRG_583:g.23121_23125delinsTGTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1136-8_1136-4delinsTGTTG MANE Select	ENSP00000384957.2:n.1136-8_1136-4delinsTG...
ENST00000264692.8:c.974-8_974-4delinsTGTTG	ENSP00000264692.5:n.974-8_974-4delinsTGTT...
ENST00000403665.6:c.1136-8_1136-4delinsTGTTG	ENSP00000384957.2:n.1136-8_1136-4delinsTG...
NM_000128.3:c.1136-8_1136-4delinsTGTTG , LRG_583t1:c.1136-8_1136-4delinsTGTTG	NP_000119.1:n.1136-8_1136-4delinsTGTTG
XM_005262821.2:c.1139-8_1139-4delinsTGTTG	XP_005262878.1:n.1139-8_1139-4delinsTGTTG...
XM_005262822.2:c.1139-8_1139-4delinsTGTTG	XP_005262879.1:n.1139-8_1139-4delinsTGTTG...
XM_005262823.2:c.869-8_869-4delinsTGTTG	XP_005262880.1:n.869-8_869-4delinsTGTTG
XM_005262824.1:c.1139-8_1139-4delinsTGTTG	XP_005262881.1:n.1139-8_1139-4delinsTGTTG...
XM_006714137.1:c.1091-8_1091-4delinsTGTTG	XP_006714200.1:n.1091-8_1091-4delinsTGTTG...
XR_938706.1:n.1544-8_1544-4delinsTGTTG
XR_938707.1:n.1544-8_1544-4delinsTGTTG
XM_005262821.4:c.1139-8_1139-4delinsTGTTG	XP_005262878.1:n.1139-8_1139-4delinsTGTTG...
XM_005262822.4:c.1139-8_1139-4delinsTGTTG	XP_005262879.1:n.1139-8_1139-4delinsTGTTG...
XM_005262823.4:c.869-8_869-4delinsTGTTG	XP_005262880.1:n.869-8_869-4delinsTGTTG
XM_006714137.3:c.1091-8_1091-4delinsTGTTG	XP_006714200.1:n.1091-8_1091-4delinsTGTTG...
XM_017007884.2:c.*2100_*2104delinsTGTTG	XP_016863373.1:n.*2100_*2104delinsTGTTG
XM_017007885.2:c.*4-8_*4-4delinsTGTTG	XP_016863374.1:n.*4-8_*4-4delinsTGTTG
XR_001741172.2:n.1610-8_1610-4delinsTGTTG
NM_000128.4:c.1136-8_1136-4delinsTGTTG MANE Select	NP_000119.1:n.1136-8_1136-4delinsTGTTG