Canonical Allele Identifier: CA557396107

Gene: F11

Linked Data

• dbSNP Id: rs1281804215
• gnomAD v2: 4-187197557-CAAGT-C
• gnomAD v3: 4-186276403-CAAGT-C
• gnomAD v4: 4-186276403-CAAGT-C
• MyVariant Identifiers: chr4:g.187197558_187197561del (hg19) ; chr4:g.186276404_186276407del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276407_186276410del , CM000666.2:g.186276407_186276410del	GRCh38
NC_000004.11:g.187197561_187197564del , CM000666.1:g.187197561_187197564del	GRCh37
NC_000004.10:g.187434555_187434558del	NCBI36
NG_008051.1:g.15444_15447del , LRG_583:g.15444_15447del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.755+17_755+20del MANE Select	ENSP00000384957.2:n.755+17_755+20del
ENST00000264692.8:c.593+17_593+20del	ENSP00000264692.5:n.593+17_593+20del
ENST00000403665.6:c.755+17_755+20del	ENSP00000384957.2:n.755+17_755+20del
ENST00000452239.1:c.202+17_202+20del
NM_000128.3:c.755+17_755+20del , LRG_583t1:c.755+17_755+20del	NP_000119.1:n.755+17_755+20del
XM_005262821.2:c.755+17_755+20del	XP_005262878.1:n.755+17_755+20del
XM_005262822.2:c.755+17_755+20del	XP_005262879.1:n.755+17_755+20del
XM_005262823.2:c.485+2132_485+2135del	XP_005262880.1:n.485+2132_485+2135del
XM_005262824.1:c.755+17_755+20del	XP_005262881.1:n.755+17_755+20del
XM_006714137.1:c.755+17_755+20del	XP_006714200.1:n.755+17_755+20del
XR_938706.1:n.1107+17_1107+20del
XR_938707.1:n.1107+17_1107+20del
XM_005262821.4:c.755+17_755+20del	XP_005262878.1:n.755+17_755+20del
XM_005262822.4:c.755+17_755+20del	XP_005262879.1:n.755+17_755+20del
XM_005262823.4:c.485+2132_485+2135del	XP_005262880.1:n.485+2132_485+2135del
XM_006714137.3:c.755+17_755+20del	XP_006714200.1:n.755+17_755+20del
XM_017007884.2:c.755+17_755+20del	XP_016863373.1:n.755+17_755+20del
XM_017007885.2:c.755+17_755+20del	XP_016863374.1:n.755+17_755+20del
XM_017007886.2:c.755+17_755+20del	XP_016863375.1:n.755+17_755+20del
XR_001741172.2:n.1088+17_1088+20del
NM_000128.4:c.755+17_755+20del MANE Select	NP_000119.1:n.755+17_755+20del