Canonical Allele Identifier: CA358943107

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187206836A>C (hg19) ; chr4:g.186285682A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285682A>C , CM000666.2:g.186285682A>C	GRCh38
NC_000004.11:g.187206836A>C , CM000666.1:g.187206836A>C	GRCh37
NC_000004.10:g.187443830A>C	NCBI36
NG_008051.1:g.24719A>C , LRG_583:g.24719A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1349A>C MANE Select	ENSP00000384957.2:p.Asn450Thr
ENST00000264691.4:c.45A>C
ENST00000264692.8:c.1187A>C	ENSP00000264692.5:p.Asn396Thr
ENST00000403665.6:c.1349A>C	ENSP00000384957.2:p.Asn450Thr
NM_000128.3:c.1349A>C , LRG_583t1:c.1349A>C	NP_000119.1:p.Asn450Thr
XM_005262821.2:c.1352A>C	XP_005262878.1:p.Asn451Thr
XM_005262822.2:c.1352A>C	XP_005262879.1:p.Asn451Thr
XM_005262823.2:c.1082A>C	XP_005262880.1:p.Asn361Thr
XM_005262824.1:c.1352A>C	XP_005262881.1:p.Asn451Thr
XM_006714137.1:c.1304A>C	XP_006714200.1:p.Asn435Thr
XR_938706.1:n.1757A>C
XR_938707.1:n.1757A>C
XM_005262821.4:c.1352A>C	XP_005262878.1:p.Asn451Thr
XM_005262822.4:c.1352A>C	XP_005262879.1:p.Asn451Thr
XM_005262823.4:c.1082A>C	XP_005262880.1:p.Asn361Thr
XM_006714137.3:c.1304A>C	XP_006714200.1:p.Asn435Thr
XR_001741172.2:n.1823A>C
NM_000128.4:c.1349A>C MANE Select	NP_000119.1:p.Asn450Thr