Canonical Allele Identifier: CA1519938000

Gene: F11

Linked Data

• dbSNP Id: rs1741055948

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284641_186284642insTGCG , CM000666.2:g.186284641_186284642insTGCG	GRCh38
NC_000004.11:g.187205795_187205796insTGCG , CM000666.1:g.187205795_187205796insTGCG	GRCh37
NC_000004.10:g.187442789_187442790insTGCG	NCBI36
NG_008051.1:g.23678_23679insTGCG , LRG_583:g.23678_23679insTGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+381_1304+382insTGCG MANE Select	ENSP00000384957.2:n.1304+381_1304+382insTGCG
ENST00000264692.8:c.1142+381_1142+382insTGCG	ENSP00000264692.5:n.1142+381_1142+382insTGCG
ENST00000403665.6:c.1304+381_1304+382insTGCG	ENSP00000384957.2:n.1304+381_1304+382insTGCG
NM_000128.3:c.1304+381_1304+382insTGCG , LRG_583t1:c.1304+381_1304+382insTGCG	NP_000119.1:n.1304+381_1304+382insTGCG
XM_005262821.2:c.1307+381_1307+382insTGCG	XP_005262878.1:n.1307+381_1307+382insTGCG
XM_005262822.2:c.1307+381_1307+382insTGCG	XP_005262879.1:n.1307+381_1307+382insTGCG
XM_005262823.2:c.1037+381_1037+382insTGCG	XP_005262880.1:n.1037+381_1037+382insTGCG
XM_005262824.1:c.1307+381_1307+382insTGCG	XP_005262881.1:n.1307+381_1307+382insTGCG
XM_006714137.1:c.1259+381_1259+382insTGCG	XP_006714200.1:n.1259+381_1259+382insTGCG
XR_938706.1:n.1712+381_1712+382insTGCG
XR_938707.1:n.1712+381_1712+382insTGCG
XM_005262821.4:c.1307+381_1307+382insTGCG	XP_005262878.1:n.1307+381_1307+382insTGCG
XM_005262822.4:c.1307+381_1307+382insTGCG	XP_005262879.1:n.1307+381_1307+382insTGCG
XM_005262823.4:c.1037+381_1037+382insTGCG	XP_005262880.1:n.1037+381_1037+382insTGCG
XM_006714137.3:c.1259+381_1259+382insTGCG	XP_006714200.1:n.1259+381_1259+382insTGCG
XR_001741172.2:n.1778+381_1778+382insTGCG
NM_000128.4:c.1304+381_1304+382insTGCG MANE Select	NP_000119.1:n.1304+381_1304+382insTGCG