Canonical Allele Identifier: CA2672903252

Gene: F11

Linked Data

• gnomAD v4: 4-186286019-A-AGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286020_186286022dup , CM000666.2:g.186286020_186286022dup	GRCh38
NC_000004.11:g.187207174_187207176dup , CM000666.1:g.187207174_187207176dup	GRCh37
NC_000004.10:g.187444168_187444170dup	NCBI36
NG_008051.1:g.25057_25059dup , LRG_583:g.25057_25059dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1480+207_1480+209dup MANE Select	ENSP00000384957.2:n.1480+207_1480+209dup
ENST00000264691.4:c.176+207_176+209dup
ENST00000264692.8:c.1318+207_1318+209dup	ENSP00000264692.5:n.1318+207_1318+209dup
ENST00000403665.6:c.1480+207_1480+209dup	ENSP00000384957.2:n.1480+207_1480+209dup
NM_000128.3:c.1480+207_1480+209dup , LRG_583t1:c.1480+207_1480+209dup	NP_000119.1:n.1480+207_1480+209dup
XM_005262821.2:c.1483+207_1483+209dup	XP_005262878.1:n.1483+207_1483+209dup
XM_005262822.2:c.1483+207_1483+209dup	XP_005262879.1:n.1483+207_1483+209dup
XM_005262823.2:c.1213+207_1213+209dup	XP_005262880.1:n.1213+207_1213+209dup
XM_005262824.1:c.1483+207_1483+209dup	XP_005262881.1:n.1483+207_1483+209dup
XM_006714137.1:c.1435+207_1435+209dup	XP_006714200.1:n.1435+207_1435+209dup
XR_938706.1:n.1888+207_1888+209dup
XR_938707.1:n.1888+207_1888+209dup
XM_005262821.4:c.1483+207_1483+209dup	XP_005262878.1:n.1483+207_1483+209dup
XM_005262822.4:c.1483+207_1483+209dup	XP_005262879.1:n.1483+207_1483+209dup
XM_005262823.4:c.1213+207_1213+209dup	XP_005262880.1:n.1213+207_1213+209dup
XM_006714137.3:c.1435+207_1435+209dup	XP_006714200.1:n.1435+207_1435+209dup
XR_001741172.2:n.1954+207_1954+209dup
NM_000128.4:c.1480+207_1480+209dup MANE Select	NP_000119.1:n.1480+207_1480+209dup