Canonical Allele Identifier: CA792317424

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1231620523
• gnomAD v3: 4-186288220-CAT-C
• gnomAD v4: 4-186288220-CAT-C
• MyVariant Identifiers: chr4:g.187209375_187209376del (hg19) ; chr4:g.186288221_186288222del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288221_186288222del , CM000666.2:g.186288221_186288222del	GRCh38
NC_000004.11:g.187209375_187209376del , CM000666.1:g.187209375_187209376del	GRCh37
NC_000004.10:g.187446369_187446370del	NCBI36
NG_008051.1:g.27258_27259del , LRG_583:g.27258_27259del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1717-232_1717-231del (F11) MANE Select	ENSP00000384957.2:n.1717-232_1717-231del
ENST00000264691.4:c.317-232_317-231del (F11)
ENST00000264692.8:c.1555-232_1555-231del (F11)	ENSP00000264692.5:n.1555-232_1555-231del
ENST00000403665.6:c.1717-232_1717-231del (F11)	ENSP00000384957.2:n.1717-232_1717-231del
ENST00000503841.1:n.236-232_236-231del (F11)
NM_000128.3:c.1717-232_1717-231del , LRG_583t1:c.1717-232_1717-231del (F11)	NP_000119.1:n.1717-232_1717-231del
NR_033900.1:n.1066+206_1066+207del (F11-AS1)
XM_005262821.2:c.1720-232_1720-231del (F11)	XP_005262878.1:n.1720-232_1720-231del
XM_005262822.2:c.1624-232_1624-231del (F11)	XP_005262879.1:n.1624-232_1624-231del
XM_005262823.2:c.1450-232_1450-231del (F11)	XP_005262880.1:n.1450-232_1450-231del
XM_006714137.1:c.1672-232_1672-231del (F11)	XP_006714200.1:n.1672-232_1672-231del
XM_005262821.4:c.1720-232_1720-231del (F11)	XP_005262878.1:n.1720-232_1720-231del
XM_005262822.4:c.1624-232_1624-231del (F11)	XP_005262879.1:n.1624-232_1624-231del
XM_005262823.4:c.1450-232_1450-231del (F11)	XP_005262880.1:n.1450-232_1450-231del
XM_006714137.3:c.1672-232_1672-231del (F11)	XP_006714200.1:n.1672-232_1672-231del
NM_000128.4:c.1717-232_1717-231del (F11) MANE Select	NP_000119.1:n.1717-232_1717-231del