Canonical Allele Identifier: CA1071927126

Gene: F11

Linked Data

• dbSNP Id: rs1741056979
• gnomAD v3: 4-186284644-T-TGC
• gnomAD v4: 4-186284644-T-TGC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284645_186284646insCG , CM000666.2:g.186284645_186284646insCG	GRCh38
NC_000004.11:g.187205799_187205800insCG , CM000666.1:g.187205799_187205800insCG	GRCh37
NC_000004.10:g.187442793_187442794insCG	NCBI36
NG_008051.1:g.23682_23683insCG , LRG_583:g.23682_23683insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+385_1304+386insCG MANE Select	ENSP00000384957.2:n.1304+385_1304+386insCG
ENST00000264692.8:c.1142+385_1142+386insCG	ENSP00000264692.5:n.1142+385_1142+386insCG
ENST00000403665.6:c.1304+385_1304+386insCG	ENSP00000384957.2:n.1304+385_1304+386insCG
NM_000128.3:c.1304+385_1304+386insCG , LRG_583t1:c.1304+385_1304+386insCG	NP_000119.1:n.1304+385_1304+386insCG
XM_005262821.2:c.1307+385_1307+386insCG	XP_005262878.1:n.1307+385_1307+386insCG
XM_005262822.2:c.1307+385_1307+386insCG	XP_005262879.1:n.1307+385_1307+386insCG
XM_005262823.2:c.1037+385_1037+386insCG	XP_005262880.1:n.1037+385_1037+386insCG
XM_005262824.1:c.1307+385_1307+386insCG	XP_005262881.1:n.1307+385_1307+386insCG
XM_006714137.1:c.1259+385_1259+386insCG	XP_006714200.1:n.1259+385_1259+386insCG
XR_938706.1:n.1712+385_1712+386insCG
XR_938707.1:n.1712+385_1712+386insCG
XM_005262821.4:c.1307+385_1307+386insCG	XP_005262878.1:n.1307+385_1307+386insCG
XM_005262822.4:c.1307+385_1307+386insCG	XP_005262879.1:n.1307+385_1307+386insCG
XM_005262823.4:c.1037+385_1037+386insCG	XP_005262880.1:n.1037+385_1037+386insCG
XM_006714137.3:c.1259+385_1259+386insCG	XP_006714200.1:n.1259+385_1259+386insCG
XR_001741172.2:n.1778+385_1778+386insCG
NM_000128.4:c.1304+385_1304+386insCG MANE Select	NP_000119.1:n.1304+385_1304+386insCG