Canonical Allele Identifier: CA2764868327

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186265947del , CM000666.2:g.186265947del	GRCh38
NC_000004.11:g.187187101del , CM000666.1:g.187187101del	GRCh37
NC_000004.10:g.187424095del	NCBI36
NG_008051.1:g.4984del , LRG_583:g.4984del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.6:c.-350del	ENSP00000384957.2:n.-350del
XM_005262821.2:c.-350del	XP_005262878.1:n.-350del
XM_005262822.2:c.-350del	XP_005262879.1:n.-350del
XM_005262823.2:c.-350del	XP_005262880.1:n.-350del
XM_005262824.1:c.-350del	XP_005262881.1:n.-350del
XM_006714137.1:c.-350del	XP_006714200.1:n.-350del
XR_938706.1:n.3del
XR_938707.1:n.3del