Canonical Allele Identifier: CA1519933148

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186273958_186273963delinsCTTCCA , CM000666.2:g.186273958_186273963delinsCTTCCA	GRCh38
NC_000004.11:g.187195112_187195117delinsCTTCCA , CM000666.1:g.187195112_187195117delinsCTTCCA	GRCh37
NC_000004.10:g.187432106_187432111delinsCTTCCA	NCBI36
NG_008051.1:g.12995_13000delinsCTTCCA , LRG_583:g.12995_13000delinsCTTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.326-158_326-153delinsCTTCCA MANE Select	ENSP00000384957.2:n.326-158_326-153delinsCTTCCA
ENST00000264692.8:c.323+783_323+788delinsCTTCCA	ENSP00000264692.5:n.323+783_323+788delinsCTTCCA
ENST00000403665.6:c.326-158_326-153delinsCTTCCA	ENSP00000384957.2:n.326-158_326-153delinsCTTCCA
ENST00000492972.6:c.326-158_326-153delinsCTTCCA	ENSP00000424479.1:n.326-158_326-153delinsCTTCCA
ENST00000514715.1:n.198-158_198-153delinsCTTCCA
NM_000128.3:c.326-158_326-153delinsCTTCCA , LRG_583t1:c.326-158_326-153delinsCTTCCA	NP_000119.1:n.326-158_326-153delinsCTTCCA
XM_005262821.2:c.326-158_326-153delinsCTTCCA	XP_005262878.1:n.326-158_326-153delinsCTTCCA
XM_005262822.2:c.326-158_326-153delinsCTTCCA	XP_005262879.1:n.326-158_326-153delinsCTTCCA
XM_005262823.2:c.326-158_326-153delinsCTTCCA	XP_005262880.1:n.326-158_326-153delinsCTTCCA
XM_005262824.1:c.326-158_326-153delinsCTTCCA	XP_005262881.1:n.326-158_326-153delinsCTTCCA
XM_006714137.1:c.326-158_326-153delinsCTTCCA	XP_006714200.1:n.326-158_326-153delinsCTTCCA
XR_938706.1:n.678-158_678-153delinsCTTCCA
XR_938707.1:n.678-158_678-153delinsCTTCCA
NM_001354804.1:c.326-158_326-153delinsCTTCCA	NP_001341733.1:n.326-158_326-153delinsCTTCCA
XM_005262821.4:c.326-158_326-153delinsCTTCCA	XP_005262878.1:n.326-158_326-153delinsCTTCCA
XM_005262822.4:c.326-158_326-153delinsCTTCCA	XP_005262879.1:n.326-158_326-153delinsCTTCCA
XM_005262823.4:c.326-158_326-153delinsCTTCCA	XP_005262880.1:n.326-158_326-153delinsCTTCCA
XM_006714137.3:c.326-158_326-153delinsCTTCCA	XP_006714200.1:n.326-158_326-153delinsCTTCCA
XM_017007884.2:c.326-158_326-153delinsCTTCCA	XP_016863373.1:n.326-158_326-153delinsCTTCCA
XM_017007885.2:c.326-158_326-153delinsCTTCCA	XP_016863374.1:n.326-158_326-153delinsCTTCCA
XM_017007886.2:c.326-158_326-153delinsCTTCCA	XP_016863375.1:n.326-158_326-153delinsCTTCCA
XR_001741172.2:n.659-158_659-153delinsCTTCCA
NM_000128.4:c.326-158_326-153delinsCTTCCA MANE Select	NP_000119.1:n.326-158_326-153delinsCTTCCA
NM_001354804.2:c.326-158_326-153delinsCTTCCA	NP_001341733.1:n.326-158_326-153delinsCTTCCA