Canonical Allele Identifier: CA442639126

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205388A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284234A>T , CM000666.2:g.186284234A>T	GRCh38
NC_000004.11:g.187205388A>T , CM000666.1:g.187205388A>T	GRCh37
NC_000004.10:g.187442382A>T	NCBI36
NG_008051.1:g.23271A>T , LRG_583:g.23271A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1278A>T MANE Select	ENSP00000384957.2:p.Ile426=
ENST00000264692.8:c.1116A>T	ENSP00000264692.5:p.Ile372=
ENST00000403665.6:c.1278A>T	ENSP00000384957.2:p.Ile426=
NM_000128.3:c.1278A>T , LRG_583t1:c.1278A>T	NP_000119.1:p.Ile426=
XM_005262821.2:c.1281A>T	XP_005262878.1:p.Ile427=
XM_005262822.2:c.1281A>T	XP_005262879.1:p.Ile427=
XM_005262823.2:c.1011A>T	XP_005262880.1:p.Ile337=
XM_005262824.1:c.1281A>T	XP_005262881.1:p.Ile427=
XM_006714137.1:c.1233A>T	XP_006714200.1:p.Ile411=
XR_938706.1:n.1686A>T
XR_938707.1:n.1686A>T
XM_005262821.4:c.1281A>T	XP_005262878.1:p.Ile427=
XM_005262822.4:c.1281A>T	XP_005262879.1:p.Ile427=
XM_005262823.4:c.1011A>T	XP_005262880.1:p.Ile337=
XM_006714137.3:c.1233A>T	XP_006714200.1:p.Ile411=
XR_001741172.2:n.1752A>T
NM_000128.4:c.1278A>T MANE Select	NP_000119.1:p.Ile426=