Canonical Allele Identifier: CA358945679

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187208942G>C (hg19) ; chr4:g.186287788G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287788G>C , CM000666.2:g.186287788G>C	GRCh38
NC_000004.11:g.187208942G>C , CM000666.1:g.187208942G>C	GRCh37
NC_000004.10:g.187445936G>C	NCBI36
NG_008051.1:g.26825G>C , LRG_583:g.26825G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1681G>C (F11) MANE Select	ENSP00000384957.2:p.Ala561Pro
ENST00000264691.4:c.281G>C (F11)
ENST00000264692.8:c.1519G>C (F11)	ENSP00000264692.5:p.Ala507Pro
ENST00000403665.6:c.1681G>C (F11)	ENSP00000384957.2:p.Ala561Pro
ENST00000503841.1:n.200G>C (F11)
NM_000128.3:c.1681G>C , LRG_583t1:c.1681G>C (F11)	NP_000119.1:p.Ala561Pro
NR_033900.1:n.1066+640C>G (F11-AS1)
XM_005262821.2:c.1684G>C (F11)	XP_005262878.1:p.Ala562Pro
XM_005262822.2:c.1588G>C (F11)	XP_005262879.1:p.Ala530Pro
XM_005262823.2:c.1414G>C (F11)	XP_005262880.1:p.Ala472Pro
XM_006714137.1:c.1636G>C (F11)	XP_006714200.1:p.Ala546Pro
XM_005262821.4:c.1684G>C (F11)	XP_005262878.1:p.Ala562Pro
XM_005262822.4:c.1588G>C (F11)	XP_005262879.1:p.Ala530Pro
XM_005262823.4:c.1414G>C (F11)	XP_005262880.1:p.Ala472Pro
XM_006714137.3:c.1636G>C (F11)	XP_006714200.1:p.Ala546Pro
NM_000128.4:c.1681G>C (F11) MANE Select	NP_000119.1:p.Ala561Pro