Canonical Allele Identifier: CA1519939477

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287862T= , CM000666.2:g.186287862T= GRCh38
NC_000004.11:g.187209016T= , CM000666.1:g.187209016T= GRCh37
NC_000004.10:g.187446010T= NCBI36
NG_008051.1:g.26899T= , LRG_583:g.26899T=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1716+39T= (F11) MANE Select ENSP00000384957.2:n.1716+39T=
ENST00000264691.4:c.316+39T= (F11)
ENST00000264692.8:c.1554+39T= (F11) ENSP00000264692.5:n.1554+39T=
ENST00000403665.6:c.1716+39T= (F11) ENSP00000384957.2:n.1716+39T=
ENST00000503841.1:n.235+39T= (F11)
NM_000128.3:c.1716+39T= , LRG_583t1:c.1716+39T= (F11) NP_000119.1:n.1716+39T=
NR_033900.1:n.1066+566A= (F11-AS1)
XM_005262821.2:c.1719+39T= (F11) XP_005262878.1:n.1719+39T=
XM_005262822.2:c.1623+39T= (F11) XP_005262879.1:n.1623+39T=
XM_005262823.2:c.1449+39T= (F11) XP_005262880.1:n.1449+39T=
XM_006714137.1:c.1671+39T= (F11) XP_006714200.1:n.1671+39T=
XM_005262821.4:c.1719+39T= (F11) XP_005262878.1:n.1719+39T=
XM_005262822.4:c.1623+39T= (F11) XP_005262879.1:n.1623+39T=
XM_005262823.4:c.1449+39T= (F11) XP_005262880.1:n.1449+39T=
XM_006714137.3:c.1671+39T= (F11) XP_006714200.1:n.1671+39T=
NM_000128.4:c.1716+39T= (F11) MANE Select NP_000119.1:n.1716+39T=