Canonical Allele Identifier: CA1519936141

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280567_186280568delinsTA , CM000666.2:g.186280567_186280568delinsTA	GRCh38
NC_000004.11:g.187201721_187201722delinsTA , CM000666.1:g.187201721_187201722delinsTA	GRCh37
NC_000004.10:g.187438715_187438716delinsTA	NCBI36
NG_008051.1:g.19604_19605delinsTA , LRG_583:g.19604_19605delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1122_1123delinsTA MANE Select	ENSP00000384957.2:p.Cys374=
ENST00000264692.8:c.960_961delinsTA	ENSP00000264692.5:p.Cys320=
ENST00000403665.6:c.1122_1123delinsTA	ENSP00000384957.2:p.Cys374=
ENST00000452239.1:c.569_570delinsTA
NM_000128.3:c.1122_1123delinsTA , LRG_583t1:c.1122_1123delinsTA	NP_000119.1:p.Cys374=
XM_005262821.2:c.1125_1126delinsTA	XP_005262878.1:p.Cys375=
XM_005262822.2:c.1125_1126delinsTA	XP_005262879.1:p.Cys375=
XM_005262823.2:c.855_856delinsTA	XP_005262880.1:p.Cys285=
XM_005262824.1:c.1125_1126delinsTA	XP_005262881.1:p.Cys375=
XM_006714137.1:c.1077_1078delinsTA	XP_006714200.1:p.Cys359=
XR_938706.1:n.1477_1478delinsTA
XR_938707.1:n.1477_1478delinsTA
XM_005262821.4:c.1125_1126delinsTA	XP_005262878.1:p.Cys375=
XM_005262822.4:c.1125_1126delinsTA	XP_005262879.1:p.Cys375=
XM_005262823.4:c.855_856delinsTA	XP_005262880.1:p.Cys285=
XM_006714137.3:c.1077_1078delinsTA	XP_006714200.1:p.Cys359=
XM_017007884.2:c.1125_1126delinsTA	XP_016863373.1:p.Cys375=
XM_017007885.2:c.1125_1126delinsTA	XP_016863374.1:p.Cys375=
XM_017007886.2:c.1122_1123delinsTA	XP_016863375.1:p.Cys374=
XR_001741172.2:n.1543_1544delinsTA
NM_000128.4:c.1122_1123delinsTA MANE Select	NP_000119.1:p.Cys374=