Canonical Allele Identifier: CA442640060

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187206885A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285731A>T , CM000666.2:g.186285731A>T	GRCh38
NC_000004.11:g.187206885A>T , CM000666.1:g.187206885A>T	GRCh37
NC_000004.10:g.187443879A>T	NCBI36
NG_008051.1:g.24768A>T , LRG_583:g.24768A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1398A>T MANE Select	ENSP00000384957.2:p.Ile466=
ENST00000264691.4:c.94A>T
ENST00000264692.8:c.1236A>T	ENSP00000264692.5:p.Ile412=
ENST00000403665.6:c.1398A>T	ENSP00000384957.2:p.Ile466=
NM_000128.3:c.1398A>T , LRG_583t1:c.1398A>T	NP_000119.1:p.Ile466=
XM_005262821.2:c.1401A>T	XP_005262878.1:p.Ile467=
XM_005262822.2:c.1401A>T	XP_005262879.1:p.Ile467=
XM_005262823.2:c.1131A>T	XP_005262880.1:p.Ile377=
XM_005262824.1:c.1401A>T	XP_005262881.1:p.Ile467=
XM_006714137.1:c.1353A>T	XP_006714200.1:p.Ile451=
XR_938706.1:n.1806A>T
XR_938707.1:n.1806A>T
XM_005262821.4:c.1401A>T	XP_005262878.1:p.Ile467=
XM_005262822.4:c.1401A>T	XP_005262879.1:p.Ile467=
XM_005262823.4:c.1131A>T	XP_005262880.1:p.Ile377=
XM_006714137.3:c.1353A>T	XP_006714200.1:p.Ile451=
XR_001741172.2:n.1872A>T
NM_000128.4:c.1398A>T MANE Select	NP_000119.1:p.Ile466=