Canonical Allele Identifier: CA1519938833

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286477_186286479delinsTGG , CM000666.2:g.186286477_186286479delinsTGG	GRCh38
NC_000004.11:g.187207631_187207633delinsTGG , CM000666.1:g.187207631_187207633delinsTGG	GRCh37
NC_000004.10:g.187444625_187444627delinsTGG	NCBI36
NG_008051.1:g.25514_25516delinsTGG , LRG_583:g.25514_25516delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1543_1545delinsTGG (F11) MANE Select	ENSP00000384957.2:p.Trp515=
ENST00000264691.4:c.176+664_176+666delinsTGG (F11)
ENST00000264692.8:c.1381_1383delinsTGG (F11)	ENSP00000264692.5:p.Trp461=
ENST00000403665.6:c.1543_1545delinsTGG (F11)	ENSP00000384957.2:p.Trp515=
NM_000128.3:c.1543_1545delinsTGG , LRG_583t1:c.1543_1545delinsTGG (F11)	NP_000119.1:p.Trp515=
NR_033900.1:n.1067-213_1067-211delinsCCA (F11-AS1)
XM_005262821.2:c.1546_1548delinsTGG (F11)	XP_005262878.1:p.Trp516=
XM_005262822.2:c.1483+664_1483+666delinsTGG (F11)	XP_005262879.1:n.1483+664_1483+666delinsTGG
XM_005262823.2:c.1276_1278delinsTGG (F11)	XP_005262880.1:p.Trp426=
XM_005262824.1:c.1484-69_1484-67delinsTGG (F11)	XP_005262881.1:n.1484-69_1484-67delinsTGG
XM_006714137.1:c.1498_1500delinsTGG (F11)	XP_006714200.1:p.Trp500=
XR_938706.1:n.1951_1953delinsTGG (F11)
XR_938707.1:n.1888+664_1888+666delinsTGG (F11)
XM_005262821.4:c.1546_1548delinsTGG (F11)	XP_005262878.1:p.Trp516=
XM_005262822.4:c.1483+664_1483+666delinsTGG (F11)	XP_005262879.1:n.1483+664_1483+666delinsTGG
XM_005262823.4:c.1276_1278delinsTGG (F11)	XP_005262880.1:p.Trp426=
XM_006714137.3:c.1498_1500delinsTGG (F11)	XP_006714200.1:p.Trp500=
XR_001741172.2:n.2017_2019delinsTGG (F11)
NM_000128.4:c.1543_1545delinsTGG (F11) MANE Select	NP_000119.1:p.Trp515=