Canonical Allele Identifier: CA442641386

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209690T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288536T>C , CM000666.2:g.186288536T>C	GRCh38
NC_000004.11:g.187209690T>C , CM000666.1:g.187209690T>C	GRCh37
NC_000004.10:g.187446684T>C	NCBI36
NG_008051.1:g.27573T>C , LRG_583:g.27573T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1800T>C (F11) MANE Select	ENSP00000384957.2:p.Ala600=
ENST00000264691.4:c.400T>C (F11)
ENST00000264692.8:c.1638T>C (F11)	ENSP00000264692.5:p.Ala546=
ENST00000403665.6:c.1800T>C (F11)	ENSP00000384957.2:p.Ala600=
ENST00000503841.1:n.319T>C (F11)
NM_000128.3:c.1800T>C , LRG_583t1:c.1800T>C (F11)	NP_000119.1:p.Ala600=
NR_033900.1:n.958A>G (F11-AS1)
XM_005262821.2:c.1803T>C (F11)	XP_005262878.1:p.Ala601=
XM_005262822.2:c.1707T>C (F11)	XP_005262879.1:p.Ala569=
XM_005262823.2:c.1533T>C (F11)	XP_005262880.1:p.Ala511=
XM_006714137.1:c.1755T>C (F11)	XP_006714200.1:p.Ala585=
XM_005262821.4:c.1803T>C (F11)	XP_005262878.1:p.Ala601=
XM_005262822.4:c.1707T>C (F11)	XP_005262879.1:p.Ala569=
XM_005262823.4:c.1533T>C (F11)	XP_005262880.1:p.Ala511=
XM_006714137.3:c.1755T>C (F11)	XP_006714200.1:p.Ala585=
NM_000128.4:c.1800T>C (F11) MANE Select	NP_000119.1:p.Ala600=