Canonical Allele Identifier: CA442644318

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187196953A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186275799A>C , CM000666.2:g.186275799A>C	GRCh38
NC_000004.11:g.187196953A>C , CM000666.1:g.187196953A>C	GRCh37
NC_000004.10:g.187433947A>C	NCBI36
NG_008051.1:g.14836A>C , LRG_583:g.14836A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.498A>C MANE Select	ENSP00000384957.2:p.Leu166=
ENST00000264692.8:c.336A>C	ENSP00000264692.5:p.Leu112=
ENST00000403665.6:c.498A>C	ENSP00000384957.2:p.Leu166=
NM_000128.3:c.498A>C , LRG_583t1:c.498A>C	NP_000119.1:p.Leu166=
XM_005262821.2:c.498A>C	XP_005262878.1:p.Leu166=
XM_005262822.2:c.498A>C	XP_005262879.1:p.Leu166=
XM_005262823.2:c.485+1524A>C	XP_005262880.1:n.485+1524A>C
XM_005262824.1:c.498A>C	XP_005262881.1:p.Leu166=
XM_006714137.1:c.498A>C	XP_006714200.1:p.Leu166=
XR_938706.1:n.850A>C
XR_938707.1:n.850A>C
XM_005262821.4:c.498A>C	XP_005262878.1:p.Leu166=
XM_005262822.4:c.498A>C	XP_005262879.1:p.Leu166=
XM_005262823.4:c.485+1524A>C	XP_005262880.1:n.485+1524A>C
XM_006714137.3:c.498A>C	XP_006714200.1:p.Leu166=
XM_017007884.2:c.498A>C	XP_016863373.1:p.Leu166=
XM_017007885.2:c.498A>C	XP_016863374.1:p.Leu166=
XM_017007886.2:c.498A>C	XP_016863375.1:p.Leu166=
XR_001741172.2:n.831A>C
NM_000128.4:c.498A>C MANE Select	NP_000119.1:p.Leu166=