Canonical Allele Identifier: CA557055430

Gene: F11

Linked Data

• dbSNP Id: rs1561490677
• gnomAD v2: 4-187206746-AT-A
• gnomAD v4: 4-186285592-AT-A
• MyVariant Identifiers: chr4:g.187206747del (hg19) ; chr4:g.186285593del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285597del , CM000666.2:g.186285597del	GRCh38
NC_000004.11:g.187206751del , CM000666.1:g.187206751del	GRCh37
NC_000004.10:g.187443745del	NCBI36
NG_008051.1:g.24634del , LRG_583:g.24634del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1305-41del MANE Select	ENSP00000384957.2:n.1305-41del
ENST00000264692.8:c.1143-41del	ENSP00000264692.5:n.1143-41del
ENST00000403665.6:c.1305-41del	ENSP00000384957.2:n.1305-41del
NM_000128.3:c.1305-41del , LRG_583t1:c.1305-41del	NP_000119.1:n.1305-41del
XM_005262821.2:c.1308-41del	XP_005262878.1:n.1308-41del
XM_005262822.2:c.1308-41del	XP_005262879.1:n.1308-41del
XM_005262823.2:c.1038-41del	XP_005262880.1:n.1038-41del
XM_005262824.1:c.1308-41del	XP_005262881.1:n.1308-41del
XM_006714137.1:c.1260-41del	XP_006714200.1:n.1260-41del
XR_938706.1:n.1713-41del
XR_938707.1:n.1713-41del
XM_005262821.4:c.1308-41del	XP_005262878.1:n.1308-41del
XM_005262822.4:c.1308-41del	XP_005262879.1:n.1308-41del
XM_005262823.4:c.1038-41del	XP_005262880.1:n.1038-41del
XM_006714137.3:c.1260-41del	XP_006714200.1:n.1260-41del
XR_001741172.2:n.1779-41del
NM_000128.4:c.1305-41del MANE Select	NP_000119.1:n.1305-41del