Canonical Allele Identifier: CA442639124

Gene: F11

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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