Canonical Allele Identifier: CA112102771

Gene: F11

Linked Data

• dbSNP Id: rs760259660

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284635_186284636insAGTG , CM000666.2:g.186284635_186284636insAGTG	GRCh38
NC_000004.11:g.187205789_187205790insAGTG , CM000666.1:g.187205789_187205790insAGTG	GRCh37
NC_000004.10:g.187442783_187442784insAGTG	NCBI36
NG_008051.1:g.23672_23673insAGTG , LRG_583:g.23672_23673insAGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+375_1304+376insAGTG MANE Select	ENSP00000384957.2:n.1304+375_1304+376insAGTG
ENST00000264692.8:c.1142+375_1142+376insAGTG	ENSP00000264692.5:n.1142+375_1142+376insAGTG
ENST00000403665.6:c.1304+375_1304+376insAGTG	ENSP00000384957.2:n.1304+375_1304+376insAGTG
NM_000128.3:c.1304+375_1304+376insAGTG , LRG_583t1:c.1304+375_1304+376insAGTG	NP_000119.1:n.1304+375_1304+376insAGTG
XM_005262821.2:c.1307+375_1307+376insAGTG	XP_005262878.1:n.1307+375_1307+376insAGTG
XM_005262822.2:c.1307+375_1307+376insAGTG	XP_005262879.1:n.1307+375_1307+376insAGTG
XM_005262823.2:c.1037+375_1037+376insAGTG	XP_005262880.1:n.1037+375_1037+376insAGTG
XM_005262824.1:c.1307+375_1307+376insAGTG	XP_005262881.1:n.1307+375_1307+376insAGTG
XM_006714137.1:c.1259+375_1259+376insAGTG	XP_006714200.1:n.1259+375_1259+376insAGTG
XR_938706.1:n.1712+375_1712+376insAGTG
XR_938707.1:n.1712+375_1712+376insAGTG
XM_005262821.4:c.1307+375_1307+376insAGTG	XP_005262878.1:n.1307+375_1307+376insAGTG
XM_005262822.4:c.1307+375_1307+376insAGTG	XP_005262879.1:n.1307+375_1307+376insAGTG
XM_005262823.4:c.1037+375_1037+376insAGTG	XP_005262880.1:n.1037+375_1037+376insAGTG
XM_006714137.3:c.1259+375_1259+376insAGTG	XP_006714200.1:n.1259+375_1259+376insAGTG
XR_001741172.2:n.1778+375_1778+376insAGTG
NM_000128.4:c.1304+375_1304+376insAGTG MANE Select	NP_000119.1:n.1304+375_1304+376insAGTG