Canonical Allele Identifier: CA557055650

Gene: F11 F11-AS1

Linked Data

• gnomAD v2: 4-187209247-TAG-T
• MyVariant Identifiers: chr4:g.187209248_187209249del (hg19) ; chr4:g.186288094_186288095del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288094_186288095del , CM000666.2:g.186288094_186288095del	GRCh38
NC_000004.11:g.187209248_187209249del , CM000666.1:g.187209248_187209249del	GRCh37
NC_000004.10:g.187446242_187446243del	NCBI36
NG_008051.1:g.27131_27132del , LRG_583:g.27131_27132del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1716+271_1716+272del (F11) MANE Select	ENSP00000384957.2:n.1716+271_1716+272del
ENST00000264691.4:c.316+271_316+272del (F11)
ENST00000264692.8:c.1554+271_1554+272del (F11)	ENSP00000264692.5:n.1554+271_1554+272del
ENST00000403665.6:c.1716+271_1716+272del (F11)	ENSP00000384957.2:n.1716+271_1716+272del
ENST00000503841.1:n.235+271_235+272del (F11)
NM_000128.3:c.1716+271_1716+272del , LRG_583t1:c.1716+271_1716+272del (F11)	NP_000119.1:n.1716+271_1716+272del
NR_033900.1:n.1066+333_1066+334del (F11-AS1)
XM_005262821.2:c.1719+271_1719+272del (F11)	XP_005262878.1:n.1719+271_1719+272del
XM_005262822.2:c.1623+271_1623+272del (F11)	XP_005262879.1:n.1623+271_1623+272del
XM_005262823.2:c.1449+271_1449+272del (F11)	XP_005262880.1:n.1449+271_1449+272del
XM_006714137.1:c.1671+271_1671+272del (F11)	XP_006714200.1:n.1671+271_1671+272del
XM_005262821.4:c.1719+271_1719+272del (F11)	XP_005262878.1:n.1719+271_1719+272del
XM_005262822.4:c.1623+271_1623+272del (F11)	XP_005262879.1:n.1623+271_1623+272del
XM_005262823.4:c.1449+271_1449+272del (F11)	XP_005262880.1:n.1449+271_1449+272del
XM_006714137.3:c.1671+271_1671+272del (F11)	XP_006714200.1:n.1671+271_1671+272del
NM_000128.4:c.1716+271_1716+272del (F11) MANE Select	NP_000119.1:n.1716+271_1716+272del