Canonical Allele Identifier: CA1519937811
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284223A= , CM000666.2:g.186284223A= GRCh38
NC_000004.11:g.187205377A= , CM000666.1:g.187205377A= GRCh37
NC_000004.10:g.187442371A= NCBI36
NG_008051.1:g.23260A= , LRG_583:g.23260A=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1267A= MANE Select ENSP00000384957.2:p.Asn423=
ENST00000264692.8:c.1105A= ENSP00000264692.5:p.Asn369=
ENST00000403665.6:c.1267A= ENSP00000384957.2:p.Asn423=
NM_000128.3:c.1267A= , LRG_583t1:c.1267A= NP_000119.1:p.Asn423=
XM_005262821.2:c.1270A= XP_005262878.1:p.Asn424=
XM_005262822.2:c.1270A= XP_005262879.1:p.Asn424=
XM_005262823.2:c.1000A= XP_005262880.1:p.Asn334=
XM_005262824.1:c.1270A= XP_005262881.1:p.Asn424=
XM_006714137.1:c.1222A= XP_006714200.1:p.Asn408=
XR_938706.1:n.1675A=
XR_938707.1:n.1675A=
XM_005262821.4:c.1270A= XP_005262878.1:p.Asn424=
XM_005262822.4:c.1270A= XP_005262879.1:p.Asn424=
XM_005262823.4:c.1000A= XP_005262880.1:p.Asn334=
XM_006714137.3:c.1222A= XP_006714200.1:p.Asn408=
XR_001741172.2:n.1741A=
NM_000128.4:c.1267A= MANE Select NP_000119.1:p.Asn423=