Canonical Allele Identifier: CA358942106

Gene: F11

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284218T>A , CM000666.2:g.186284218T>A	GRCh38
NC_000004.11:g.187205372T>A , CM000666.1:g.187205372T>A	GRCh37
NC_000004.10:g.187442366T>A	NCBI36
NG_008051.1:g.23255T>A , LRG_583:g.23255T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1262T>A MANE Select	ENSP00000384957.2:p.Ile421Asn
ENST00000264692.8:c.1100T>A	ENSP00000264692.5:p.Ile367Asn
ENST00000403665.6:c.1262T>A	ENSP00000384957.2:p.Ile421Asn
NM_000128.3:c.1262T>A , LRG_583t1:c.1262T>A	NP_000119.1:p.Ile421Asn
XM_005262821.2:c.1265T>A	XP_005262878.1:p.Ile422Asn
XM_005262822.2:c.1265T>A	XP_005262879.1:p.Ile422Asn
XM_005262823.2:c.995T>A	XP_005262880.1:p.Ile332Asn
XM_005262824.1:c.1265T>A	XP_005262881.1:p.Ile422Asn
XM_006714137.1:c.1217T>A	XP_006714200.1:p.Ile406Asn
XR_938706.1:n.1670T>A
XR_938707.1:n.1670T>A
XM_005262821.4:c.1265T>A	XP_005262878.1:p.Ile422Asn
XM_005262822.4:c.1265T>A	XP_005262879.1:p.Ile422Asn
XM_005262823.4:c.995T>A	XP_005262880.1:p.Ile332Asn
XM_006714137.3:c.1217T>A	XP_006714200.1:p.Ile406Asn
XR_001741172.2:n.1736T>A
NM_000128.4:c.1262T>A MANE Select	NP_000119.1:p.Ile421Asn