Canonical Allele Identifier: CA1519938845

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186286506A= , CM000666.2:g.186286506A= GRCh38
NC_000004.11:g.187207660A= , CM000666.1:g.187207660A= GRCh37
NC_000004.10:g.187444654A= NCBI36
NG_008051.1:g.25543A= , LRG_583:g.25543A=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1572A= (F11) MANE Select ENSP00000384957.2:p.Leu524=
ENST00000264691.4:c.176+693A= (F11)
ENST00000264692.8:c.1410A= (F11) ENSP00000264692.5:p.Leu470=
ENST00000403665.6:c.1572A= (F11) ENSP00000384957.2:p.Leu524=
NM_000128.3:c.1572A= , LRG_583t1:c.1572A= (F11) NP_000119.1:p.Leu524=
NR_033900.1:n.1067-240T= (F11-AS1)
XM_005262821.2:c.1575A= (F11) XP_005262878.1:p.Leu525=
XM_005262822.2:c.1483+693A= (F11) XP_005262879.1:n.1483+693A=
XM_005262823.2:c.1305A= (F11) XP_005262880.1:p.Leu435=
XM_005262824.1:c.1484-40A= (F11) XP_005262881.1:n.1484-40A=
XM_006714137.1:c.1527A= (F11) XP_006714200.1:p.Leu509=
XR_938706.1:n.1980A= (F11)
XR_938707.1:n.1888+693A= (F11)
XM_005262821.4:c.1575A= (F11) XP_005262878.1:p.Leu525=
XM_005262822.4:c.1483+693A= (F11) XP_005262879.1:n.1483+693A=
XM_005262823.4:c.1305A= (F11) XP_005262880.1:p.Leu435=
XM_006714137.3:c.1527A= (F11) XP_006714200.1:p.Leu509=
NM_000128.4:c.1572A= (F11) MANE Select NP_000119.1:p.Leu524=