Canonical Allele Identifier: CA442639038

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205328C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284174C>T , CM000666.2:g.186284174C>T	GRCh38
NC_000004.11:g.187205328C>T , CM000666.1:g.187205328C>T	GRCh37
NC_000004.10:g.187442322C>T	NCBI36
NG_008051.1:g.23211C>T , LRG_583:g.23211C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1218C>T MANE Select	ENSP00000384957.2:p.His406=
ENST00000264692.8:c.1056C>T	ENSP00000264692.5:p.His352=
ENST00000403665.6:c.1218C>T	ENSP00000384957.2:p.His406=
NM_000128.3:c.1218C>T , LRG_583t1:c.1218C>T	NP_000119.1:p.His406=
XM_005262821.2:c.1221C>T	XP_005262878.1:p.His407=
XM_005262822.2:c.1221C>T	XP_005262879.1:p.His407=
XM_005262823.2:c.951C>T	XP_005262880.1:p.His317=
XM_005262824.1:c.1221C>T	XP_005262881.1:p.His407=
XM_006714137.1:c.1173C>T	XP_006714200.1:p.His391=
XR_938706.1:n.1626C>T
XR_938707.1:n.1626C>T
XM_005262821.4:c.1221C>T	XP_005262878.1:p.His407=
XM_005262822.4:c.1221C>T	XP_005262879.1:p.His407=
XM_005262823.4:c.951C>T	XP_005262880.1:p.His317=
XM_006714137.3:c.1173C>T	XP_006714200.1:p.His391=
XM_017007884.2:c.*2190C>T	XP_016863373.1:n.*2190C>T
XR_001741172.2:n.1692C>T
NM_000128.4:c.1218C>T MANE Select	NP_000119.1:p.His406=