Canonical Allele Identifier: CA2764876742

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284032C>T , CM000666.2:g.186284032C>T	GRCh38
NC_000004.11:g.187205186C>T , CM000666.1:g.187205186C>T	GRCh37
NC_000004.10:g.187442180C>T	NCBI36
NG_008051.1:g.23069C>T , LRG_583:g.23069C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1136-60C>T MANE Select	ENSP00000384957.2:n.1136-60C>T
ENST00000264692.8:c.974-60C>T	ENSP00000264692.5:n.974-60C>T
ENST00000403665.6:c.1136-60C>T	ENSP00000384957.2:n.1136-60C>T
NM_000128.3:c.1136-60C>T , LRG_583t1:c.1136-60C>T	NP_000119.1:n.1136-60C>T
XM_005262821.2:c.1139-60C>T	XP_005262878.1:n.1139-60C>T
XM_005262822.2:c.1139-60C>T	XP_005262879.1:n.1139-60C>T
XM_005262823.2:c.869-60C>T	XP_005262880.1:n.869-60C>T
XM_005262824.1:c.1139-60C>T	XP_005262881.1:n.1139-60C>T
XM_006714137.1:c.1091-60C>T	XP_006714200.1:n.1091-60C>T
XR_938706.1:n.1544-60C>T
XR_938707.1:n.1544-60C>T
XM_005262821.4:c.1139-60C>T	XP_005262878.1:n.1139-60C>T
XM_005262822.4:c.1139-60C>T	XP_005262879.1:n.1139-60C>T
XM_005262823.4:c.869-60C>T	XP_005262880.1:n.869-60C>T
XM_006714137.3:c.1091-60C>T	XP_006714200.1:n.1091-60C>T
XM_017007884.2:c.*2048C>T	XP_016863373.1:n.*2048C>T
XM_017007885.2:c.*4-60C>T	XP_016863374.1:n.*4-60C>T
XR_001741172.2:n.1610-60C>T
NM_000128.4:c.1136-60C>T MANE Select	NP_000119.1:n.1136-60C>T