Canonical Allele Identifier: CA2672901049

Gene: F11

Linked Data

• gnomAD v4: 4-186266987-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186266987_186266988insTT , CM000666.2:g.186266987_186266988insTT	GRCh38
NC_000004.11:g.187188141_187188142insTT , CM000666.1:g.187188141_187188142insTT	GRCh37
NC_000004.10:g.187425135_187425136insTT	NCBI36
NG_008051.1:g.6024_6025insTT , LRG_583:g.6024_6025insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.-1-149_-1-148insTT MANE Select	ENSP00000384957.2:n.-1-149_-1-148insTT
ENST00000264692.8:c.-1-149_-1-148insTT	ENSP00000264692.5:n.-1-149_-1-148insTT
ENST00000403665.6:c.-1-149_-1-148insTT	ENSP00000384957.2:n.-1-149_-1-148insTT
ENST00000492972.6:c.-1-149_-1-148insTT	ENSP00000424479.1:n.-1-149_-1-148insTT
NM_000128.3:c.-1-149_-1-148insTT , LRG_583t1:c.-1-149_-1-148insTT	NP_000119.1:n.-1-149_-1-148insTT
XM_005262821.2:c.-1-149_-1-148insTT	XP_005262878.1:n.-1-149_-1-148insTT
XM_005262822.2:c.-1-149_-1-148insTT	XP_005262879.1:n.-1-149_-1-148insTT
XM_005262823.2:c.-1-149_-1-148insTT	XP_005262880.1:n.-1-149_-1-148insTT
XM_005262824.1:c.-1-149_-1-148insTT	XP_005262881.1:n.-1-149_-1-148insTT
XM_006714137.1:c.-1-149_-1-148insTT	XP_006714200.1:n.-1-149_-1-148insTT
XR_938706.1:n.352-149_352-148insTT
XR_938707.1:n.352-149_352-148insTT
NM_001354804.1:c.-1-149_-1-148insTT	NP_001341733.1:n.-1-149_-1-148insTT
XM_005262821.4:c.-1-149_-1-148insTT	XP_005262878.1:n.-1-149_-1-148insTT
XM_005262822.4:c.-1-149_-1-148insTT	XP_005262879.1:n.-1-149_-1-148insTT
XM_005262823.4:c.-1-149_-1-148insTT	XP_005262880.1:n.-1-149_-1-148insTT
XM_006714137.3:c.-1-149_-1-148insTT	XP_006714200.1:n.-1-149_-1-148insTT
XM_017007884.2:c.-1-149_-1-148insTT	XP_016863373.1:n.-1-149_-1-148insTT
XM_017007885.2:c.-1-149_-1-148insTT	XP_016863374.1:n.-1-149_-1-148insTT
XM_017007886.2:c.-1-149_-1-148insTT	XP_016863375.1:n.-1-149_-1-148insTT
XR_001741172.2:n.333-149_333-148insTT
NM_000128.4:c.-1-149_-1-148insTT MANE Select	NP_000119.1:n.-1-149_-1-148insTT
NM_001354804.2:c.-1-149_-1-148insTT	NP_001341733.1:n.-1-149_-1-148insTT