Canonical Allele Identifier: CA1519939334

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287590A= , CM000666.2:g.186287590A= GRCh38
NC_000004.11:g.187208744A= , CM000666.1:g.187208744A= GRCh37
NC_000004.10:g.187445738A= NCBI36
NG_008051.1:g.26627A= , LRG_583:g.26627A=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1577-94A= (F11) MANE Select ENSP00000384957.2:n.1577-94A=
ENST00000264691.4:c.177-94A= (F11)
ENST00000264692.8:c.1415-94A= (F11) ENSP00000264692.5:n.1415-94A=
ENST00000403665.6:c.1577-94A= (F11) ENSP00000384957.2:n.1577-94A=
ENST00000503841.1:n.2A= (F11)
NM_000128.3:c.1577-94A= , LRG_583t1:c.1577-94A= (F11) NP_000119.1:n.1577-94A=
NR_033900.1:n.1066+838T= (F11-AS1)
XM_005262821.2:c.1580-94A= (F11) XP_005262878.1:n.1580-94A=
XM_005262822.2:c.1484-94A= (F11) XP_005262879.1:n.1484-94A=
XM_005262823.2:c.1310-94A= (F11) XP_005262880.1:n.1310-94A=
XM_006714137.1:c.1532-94A= (F11) XP_006714200.1:n.1532-94A=
XR_938706.1:n.1985-94A= (F11)
XR_938707.1:n.1889-94A= (F11)
XM_005262821.4:c.1580-94A= (F11) XP_005262878.1:n.1580-94A=
XM_005262822.4:c.1484-94A= (F11) XP_005262879.1:n.1484-94A=
XM_005262823.4:c.1310-94A= (F11) XP_005262880.1:n.1310-94A=
XM_006714137.3:c.1532-94A= (F11) XP_006714200.1:n.1532-94A=
NM_000128.4:c.1577-94A= (F11) MANE Select NP_000119.1:n.1577-94A=