Canonical Allele Identifier: CA1519934180
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186276291T= , CM000666.2:g.186276291T= GRCh38
NC_000004.11:g.187197445T= , CM000666.1:g.187197445T= GRCh37
NC_000004.10:g.187434439T= NCBI36
NG_008051.1:g.15328T= , LRG_583:g.15328T=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.656T= MANE Select ENSP00000384957.2:p.Met219=
ENST00000264692.8:c.494T= ENSP00000264692.5:p.Met165=
ENST00000403665.6:c.656T= ENSP00000384957.2:p.Met219=
ENST00000452239.1:c.103T=
NM_000128.3:c.656T= , LRG_583t1:c.656T= NP_000119.1:p.Met219=
XM_005262821.2:c.656T= XP_005262878.1:p.Met219=
XM_005262822.2:c.656T= XP_005262879.1:p.Met219=
XM_005262823.2:c.485+2016T= XP_005262880.1:n.485+2016T=
XM_005262824.1:c.656T= XP_005262881.1:p.Met219=
XM_006714137.1:c.656T= XP_006714200.1:p.Met219=
XR_938706.1:n.1008T=
XR_938707.1:n.1008T=
XM_005262821.4:c.656T= XP_005262878.1:p.Met219=
XM_005262822.4:c.656T= XP_005262879.1:p.Met219=
XM_005262823.4:c.485+2016T= XP_005262880.1:n.485+2016T=
XM_006714137.3:c.656T= XP_006714200.1:p.Met219=
XM_017007884.2:c.656T= XP_016863373.1:p.Met219=
XM_017007885.2:c.656T= XP_016863374.1:p.Met219=
XM_017007886.2:c.656T= XP_016863375.1:p.Met219=
XR_001741172.2:n.989T=
NM_000128.4:c.656T= MANE Select NP_000119.1:p.Met219=