Canonical Allele Identifier: CA1519938003

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284642_186284646delinsCGTGT , CM000666.2:g.186284642_186284646delinsCGTGT	GRCh38
NC_000004.11:g.187205796_187205800delinsCGTGT , CM000666.1:g.187205796_187205800delinsCGTGT	GRCh37
NC_000004.10:g.187442790_187442794delinsCGTGT	NCBI36
NG_008051.1:g.23679_23683delinsCGTGT , LRG_583:g.23679_23683delinsCGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+382_1304+386delinsCGTGT MANE Select	ENSP00000384957.2:n.1304+382_1304+386delinsCGTGT
ENST00000264692.8:c.1142+382_1142+386delinsCGTGT	ENSP00000264692.5:n.1142+382_1142+386delinsCGTGT
ENST00000403665.6:c.1304+382_1304+386delinsCGTGT	ENSP00000384957.2:n.1304+382_1304+386delinsCGTGT
NM_000128.3:c.1304+382_1304+386delinsCGTGT , LRG_583t1:c.1304+382_1304+386delinsCGTGT	NP_000119.1:n.1304+382_1304+386delinsCGTGT
XM_005262821.2:c.1307+382_1307+386delinsCGTGT	XP_005262878.1:n.1307+382_1307+386delinsCGTGT
XM_005262822.2:c.1307+382_1307+386delinsCGTGT	XP_005262879.1:n.1307+382_1307+386delinsCGTGT
XM_005262823.2:c.1037+382_1037+386delinsCGTGT	XP_005262880.1:n.1037+382_1037+386delinsCGTGT
XM_005262824.1:c.1307+382_1307+386delinsCGTGT	XP_005262881.1:n.1307+382_1307+386delinsCGTGT
XM_006714137.1:c.1259+382_1259+386delinsCGTGT	XP_006714200.1:n.1259+382_1259+386delinsCGTGT
XR_938706.1:n.1712+382_1712+386delinsCGTGT
XR_938707.1:n.1712+382_1712+386delinsCGTGT
XM_005262821.4:c.1307+382_1307+386delinsCGTGT	XP_005262878.1:n.1307+382_1307+386delinsCGTGT
XM_005262822.4:c.1307+382_1307+386delinsCGTGT	XP_005262879.1:n.1307+382_1307+386delinsCGTGT
XM_005262823.4:c.1037+382_1037+386delinsCGTGT	XP_005262880.1:n.1037+382_1037+386delinsCGTGT
XM_006714137.3:c.1259+382_1259+386delinsCGTGT	XP_006714200.1:n.1259+382_1259+386delinsCGTGT
XR_001741172.2:n.1778+382_1778+386delinsCGTGT
NM_000128.4:c.1304+382_1304+386delinsCGTGT MANE Select	NP_000119.1:n.1304+382_1304+386delinsCGTGT