Canonical Allele Identifier: CA358958597

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186274205A>T , CM000666.2:g.186274205A>T	GRCh38
NC_000004.11:g.187195359A>T , CM000666.1:g.187195359A>T	GRCh37
NC_000004.10:g.187432353A>T	NCBI36
NG_008051.1:g.13242A>T , LRG_583:g.13242A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000128.4:c.415A>T MANE Select	NP_000119.1:p.Arg139Ter
ENST00000403665.7:c.415A>T MANE Select	ENSP00000384957.2:p.Arg139Ter
NM_000128.3:c.415A>T , LRG_583t1:c.415A>T	NP_000119.1:p.Arg139Ter
NM_001354804.1:c.415A>T	NP_001341733.1:p.Arg139Ter
NM_001354804.2:c.415A>T	NP_001341733.1:p.Arg139Ter
ENST00000264692.8:c.323+1030A>T	ENSP00000264692.5:n.323+1030A>T
ENST00000403665.6:c.415A>T	ENSP00000384957.2:p.Arg139Ter
ENST00000492972.6:c.415A>T	ENSP00000424479.1:p.Arg139Ter
ENST00000514715.1:n.287A>T
XM_005262821.2:c.415A>T	XP_005262878.1:p.Arg139Ter
XM_005262821.4:c.415A>T	XP_005262878.1:p.Arg139Ter
XM_005262822.2:c.415A>T	XP_005262879.1:p.Arg139Ter
XM_005262822.4:c.415A>T	XP_005262879.1:p.Arg139Ter
XM_005262823.2:c.415A>T	XP_005262880.1:p.Arg139Ter
XM_005262823.4:c.415A>T	XP_005262880.1:p.Arg139Ter
XM_005262824.1:c.415A>T	XP_005262881.1:p.Arg139Ter
XM_006714137.1:c.415A>T	XP_006714200.1:p.Arg139Ter
XM_006714137.3:c.415A>T	XP_006714200.1:p.Arg139Ter
XM_017007884.2:c.415A>T	XP_016863373.1:p.Arg139Ter
XM_017007885.2:c.415A>T	XP_016863374.1:p.Arg139Ter
XM_017007886.2:c.415A>T	XP_016863375.1:p.Arg139Ter
XR_001741172.2:n.748A>T
XR_938706.1:n.767A>T
XR_938707.1:n.767A>T