Canonical Allele Identifier: CA2578250450
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186285577C>T , CM000666.2:g.186285577C>T GRCh38
NC_000004.11:g.187206731C>T , CM000666.1:g.187206731C>T GRCh37
NC_000004.10:g.187443725C>T NCBI36
NG_008051.1:g.24614C>T , LRG_583:g.24614C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1305-61C>T MANE Select ENSP00000384957.2:n.1305-61C>T
ENST00000264692.8:c.1143-61C>T ENSP00000264692.5:n.1143-61C>T
ENST00000403665.6:c.1305-61C>T ENSP00000384957.2:n.1305-61C>T
NM_000128.3:c.1305-61C>T , LRG_583t1:c.1305-61C>T NP_000119.1:n.1305-61C>T
XM_005262821.2:c.1308-61C>T XP_005262878.1:n.1308-61C>T
XM_005262822.2:c.1308-61C>T XP_005262879.1:n.1308-61C>T
XM_005262823.2:c.1038-61C>T XP_005262880.1:n.1038-61C>T
XM_005262824.1:c.1308-61C>T XP_005262881.1:n.1308-61C>T
XM_006714137.1:c.1260-61C>T XP_006714200.1:n.1260-61C>T
XR_938706.1:n.1713-61C>T
XR_938707.1:n.1713-61C>T
XM_005262821.4:c.1308-61C>T XP_005262878.1:n.1308-61C>T
XM_005262822.4:c.1308-61C>T XP_005262879.1:n.1308-61C>T
XM_005262823.4:c.1038-61C>T XP_005262880.1:n.1038-61C>T
XM_006714137.3:c.1260-61C>T XP_006714200.1:n.1260-61C>T
XR_001741172.2:n.1779-61C>T
NM_000128.4:c.1305-61C>T MANE Select NP_000119.1:n.1305-61C>T