Canonical Allele Identifier: CA1519934181
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276292G= , CM000666.2:g.186276292G= GRCh38
NC_000004.11:g.187197446G= , CM000666.1:g.187197446G= GRCh37
NC_000004.10:g.187434440G= NCBI36
NG_008051.1:g.15329G= , LRG_583:g.15329G=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.657G= MANE Select ENSP00000384957.2:p.Met219=
ENST00000264692.8:c.495G= ENSP00000264692.5:p.Met165=
ENST00000403665.6:c.657G= ENSP00000384957.2:p.Met219=
ENST00000452239.1:c.104G=
NM_000128.3:c.657G= , LRG_583t1:c.657G= NP_000119.1:p.Met219=
XM_005262821.2:c.657G= XP_005262878.1:p.Met219=
XM_005262822.2:c.657G= XP_005262879.1:p.Met219=
XM_005262823.2:c.485+2017G= XP_005262880.1:n.485+2017G=
XM_005262824.1:c.657G= XP_005262881.1:p.Met219=
XM_006714137.1:c.657G= XP_006714200.1:p.Met219=
XR_938706.1:n.1009G=
XR_938707.1:n.1009G=
XM_005262821.4:c.657G= XP_005262878.1:p.Met219=
XM_005262822.4:c.657G= XP_005262879.1:p.Met219=
XM_005262823.4:c.485+2017G= XP_005262880.1:n.485+2017G=
XM_006714137.3:c.657G= XP_006714200.1:p.Met219=
XM_017007884.2:c.657G= XP_016863373.1:p.Met219=
XM_017007885.2:c.657G= XP_016863374.1:p.Met219=
XM_017007886.2:c.657G= XP_016863375.1:p.Met219=
XR_001741172.2:n.990G=
NM_000128.4:c.657G= MANE Select NP_000119.1:p.Met219=