Canonical Allele Identifier: CA2672902600

Gene: F11

Linked Data

• gnomAD v4: 4-186285487-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285492dup , CM000666.2:g.186285492dup	GRCh38
NC_000004.11:g.187206646dup , CM000666.1:g.187206646dup	GRCh37
NC_000004.10:g.187443640dup	NCBI36
NG_008051.1:g.24529dup , LRG_583:g.24529dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1305-146dup MANE Select	ENSP00000384957.2:n.1305-146dup
ENST00000264692.8:c.1143-146dup	ENSP00000264692.5:n.1143-146dup
ENST00000403665.6:c.1305-146dup	ENSP00000384957.2:n.1305-146dup
NM_000128.3:c.1305-146dup , LRG_583t1:c.1305-146dup	NP_000119.1:n.1305-146dup
XM_005262821.2:c.1308-146dup	XP_005262878.1:n.1308-146dup
XM_005262822.2:c.1308-146dup	XP_005262879.1:n.1308-146dup
XM_005262823.2:c.1038-146dup	XP_005262880.1:n.1038-146dup
XM_005262824.1:c.1308-146dup	XP_005262881.1:n.1308-146dup
XM_006714137.1:c.1260-146dup	XP_006714200.1:n.1260-146dup
XR_938706.1:n.1713-146dup
XR_938707.1:n.1713-146dup
XM_005262821.4:c.1308-146dup	XP_005262878.1:n.1308-146dup
XM_005262822.4:c.1308-146dup	XP_005262879.1:n.1308-146dup
XM_005262823.4:c.1038-146dup	XP_005262880.1:n.1038-146dup
XM_006714137.3:c.1260-146dup	XP_006714200.1:n.1260-146dup
XR_001741172.2:n.1779-146dup
NM_000128.4:c.1305-146dup MANE Select	NP_000119.1:n.1305-146dup