Canonical Allele Identifier: CA792314665

Gene: F11

Linked Data

• dbSNP Id: rs934373662
• MyVariant Identifiers: chr4:g.187205797_187205798del (hg19) ; chr4:g.186284643_186284644del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284649_186284650del , CM000666.2:g.186284649_186284650del	GRCh38
NC_000004.11:g.187205803_187205804del , CM000666.1:g.187205803_187205804del	GRCh37
NC_000004.10:g.187442797_187442798del	NCBI36
NG_008051.1:g.23686_23687del , LRG_583:g.23686_23687del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+389_1304+390del MANE Select	ENSP00000384957.2:n.1304+389_1304+390del
ENST00000264692.8:c.1142+389_1142+390del	ENSP00000264692.5:n.1142+389_1142+390del
ENST00000403665.6:c.1304+389_1304+390del	ENSP00000384957.2:n.1304+389_1304+390del
NM_000128.3:c.1304+389_1304+390del , LRG_583t1:c.1304+389_1304+390del	NP_000119.1:n.1304+389_1304+390del
XM_005262821.2:c.1307+389_1307+390del	XP_005262878.1:n.1307+389_1307+390del
XM_005262822.2:c.1307+389_1307+390del	XP_005262879.1:n.1307+389_1307+390del
XM_005262823.2:c.1037+389_1037+390del	XP_005262880.1:n.1037+389_1037+390del
XM_005262824.1:c.1307+389_1307+390del	XP_005262881.1:n.1307+389_1307+390del
XM_006714137.1:c.1259+389_1259+390del	XP_006714200.1:n.1259+389_1259+390del
XR_938706.1:n.1712+389_1712+390del
XR_938707.1:n.1712+389_1712+390del
XM_005262821.4:c.1307+389_1307+390del	XP_005262878.1:n.1307+389_1307+390del
XM_005262822.4:c.1307+389_1307+390del	XP_005262879.1:n.1307+389_1307+390del
XM_005262823.4:c.1037+389_1037+390del	XP_005262880.1:n.1037+389_1037+390del
XM_006714137.3:c.1259+389_1259+390del	XP_006714200.1:n.1259+389_1259+390del
XR_001741172.2:n.1778+389_1778+390del
NM_000128.4:c.1304+389_1304+390del MANE Select	NP_000119.1:n.1304+389_1304+390del