Canonical Allele Identifier: CA1519939874

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288600_186288602delinsACT , CM000666.2:g.186288600_186288602delinsACT	GRCh38
NC_000004.11:g.187209754_187209756delinsACT , CM000666.1:g.187209754_187209756delinsACT	GRCh37
NC_000004.10:g.187446748_187446750delinsACT	NCBI36
NG_008051.1:g.27637_27639delinsACT , LRG_583:g.27637_27639delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1864_1866delinsACT (F11) MANE Select	ENSP00000384957.2:p.Thr622=
ENST00000264691.4:c.464_466delinsACT (F11)
ENST00000264692.8:c.1702_1704delinsACT (F11)	ENSP00000264692.5:p.Thr568=
ENST00000403665.6:c.1864_1866delinsACT (F11)	ENSP00000384957.2:p.Thr622=
ENST00000503841.1:n.383_385delinsACT (F11)
NM_000128.3:c.1864_1866delinsACT , LRG_583t1:c.1864_1866delinsACT (F11)	NP_000119.1:p.Thr622=
NR_033900.1:n.892_894delinsAGT (F11-AS1)
XM_005262821.2:c.1867_1869delinsACT (F11)	XP_005262878.1:p.Thr623=
XM_005262822.2:c.1771_1773delinsACT (F11)	XP_005262879.1:p.Thr591=
XM_005262823.2:c.1597_1599delinsACT (F11)	XP_005262880.1:p.Thr533=
XM_006714137.1:c.1819_1821delinsACT (F11)	XP_006714200.1:p.Thr607=
XM_005262821.4:c.1867_1869delinsACT (F11)	XP_005262878.1:p.Thr623=
XM_005262822.4:c.1771_1773delinsACT (F11)	XP_005262879.1:p.Thr591=
XM_005262823.4:c.1597_1599delinsACT (F11)	XP_005262880.1:p.Thr533=
XM_006714137.3:c.1819_1821delinsACT (F11)	XP_006714200.1:p.Thr607=
NM_000128.4:c.1864_1866delinsACT (F11) MANE Select	NP_000119.1:p.Thr622=