Canonical Allele Identifier: CA2533988824

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285553del , CM000666.2:g.186285553del	GRCh38
NC_000004.11:g.187206707del , CM000666.1:g.187206707del	GRCh37
NC_000004.10:g.187443701del	NCBI36
NG_008051.1:g.24590del , LRG_583:g.24590del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1305-85del MANE Select	ENSP00000384957.2:n.1305-85del
ENST00000264692.8:c.1143-85del	ENSP00000264692.5:n.1143-85del
ENST00000403665.6:c.1305-85del	ENSP00000384957.2:n.1305-85del
NM_000128.3:c.1305-85del , LRG_583t1:c.1305-85del	NP_000119.1:n.1305-85del
XM_005262821.2:c.1308-85del	XP_005262878.1:n.1308-85del
XM_005262822.2:c.1308-85del	XP_005262879.1:n.1308-85del
XM_005262823.2:c.1038-85del	XP_005262880.1:n.1038-85del
XM_005262824.1:c.1308-85del	XP_005262881.1:n.1308-85del
XM_006714137.1:c.1260-85del	XP_006714200.1:n.1260-85del
XR_938706.1:n.1713-85del
XR_938707.1:n.1713-85del
XM_005262821.4:c.1308-85del	XP_005262878.1:n.1308-85del
XM_005262822.4:c.1308-85del	XP_005262879.1:n.1308-85del
XM_005262823.4:c.1038-85del	XP_005262880.1:n.1038-85del
XM_006714137.3:c.1260-85del	XP_006714200.1:n.1260-85del
XR_001741172.2:n.1779-85del
NM_000128.4:c.1305-85del MANE Select	NP_000119.1:n.1305-85del