Canonical Allele Identifier: CA358943070

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187206830T>C (hg19) ; chr4:g.186285676T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285676T>C , CM000666.2:g.186285676T>C	GRCh38
NC_000004.11:g.187206830T>C , CM000666.1:g.187206830T>C	GRCh37
NC_000004.10:g.187443824T>C	NCBI36
NG_008051.1:g.24713T>C , LRG_583:g.24713T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1343T>C MANE Select	ENSP00000384957.2:p.Ile448Thr
ENST00000264691.4:c.39T>C
ENST00000264692.8:c.1181T>C	ENSP00000264692.5:p.Ile394Thr
ENST00000403665.6:c.1343T>C	ENSP00000384957.2:p.Ile448Thr
NM_000128.3:c.1343T>C , LRG_583t1:c.1343T>C	NP_000119.1:p.Ile448Thr
XM_005262821.2:c.1346T>C	XP_005262878.1:p.Ile449Thr
XM_005262822.2:c.1346T>C	XP_005262879.1:p.Ile449Thr
XM_005262823.2:c.1076T>C	XP_005262880.1:p.Ile359Thr
XM_005262824.1:c.1346T>C	XP_005262881.1:p.Ile449Thr
XM_006714137.1:c.1298T>C	XP_006714200.1:p.Ile433Thr
XR_938706.1:n.1751T>C
XR_938707.1:n.1751T>C
XM_005262821.4:c.1346T>C	XP_005262878.1:p.Ile449Thr
XM_005262822.4:c.1346T>C	XP_005262879.1:p.Ile449Thr
XM_005262823.4:c.1076T>C	XP_005262880.1:p.Ile359Thr
XM_006714137.3:c.1298T>C	XP_006714200.1:p.Ile433Thr
XR_001741172.2:n.1817T>C
NM_000128.4:c.1343T>C MANE Select	NP_000119.1:p.Ile448Thr