Canonical Allele Identifier: CA1519937933

Gene: F11

Linked Data

• dbSNP Id: rs1741041689

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284511G>T , CM000666.2:g.186284511G>T	GRCh38
NC_000004.11:g.187205665G>T , CM000666.1:g.187205665G>T	GRCh37
NC_000004.10:g.187442659G>T	NCBI36
NG_008051.1:g.23548G>T , LRG_583:g.23548G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+251G>T MANE Select	ENSP00000384957.2:n.1304+251G>T
ENST00000264692.8:c.1142+251G>T	ENSP00000264692.5:n.1142+251G>T
ENST00000403665.6:c.1304+251G>T	ENSP00000384957.2:n.1304+251G>T
NM_000128.3:c.1304+251G>T , LRG_583t1:c.1304+251G>T	NP_000119.1:n.1304+251G>T
XM_005262821.2:c.1307+251G>T	XP_005262878.1:n.1307+251G>T
XM_005262822.2:c.1307+251G>T	XP_005262879.1:n.1307+251G>T
XM_005262823.2:c.1037+251G>T	XP_005262880.1:n.1037+251G>T
XM_005262824.1:c.1307+251G>T	XP_005262881.1:n.1307+251G>T
XM_006714137.1:c.1259+251G>T	XP_006714200.1:n.1259+251G>T
XR_938706.1:n.1712+251G>T
XR_938707.1:n.1712+251G>T
XM_005262821.4:c.1307+251G>T	XP_005262878.1:n.1307+251G>T
XM_005262822.4:c.1307+251G>T	XP_005262879.1:n.1307+251G>T
XM_005262823.4:c.1037+251G>T	XP_005262880.1:n.1037+251G>T
XM_006714137.3:c.1259+251G>T	XP_006714200.1:n.1259+251G>T
XR_001741172.2:n.1778+251G>T
NM_000128.4:c.1304+251G>T MANE Select	NP_000119.1:n.1304+251G>T