Canonical Allele Identifier: CA1519934078

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276076_186276081delinsTTAAAA , CM000666.2:g.186276076_186276081delinsTTAAAA	GRCh38
NC_000004.11:g.187197230_187197235delinsTTAAAA , CM000666.1:g.187197230_187197235delinsTTAAAA	GRCh37
NC_000004.10:g.187434224_187434229delinsTTAAAA	NCBI36
NG_008051.1:g.15113_15118delinsTTAAAA , LRG_583:g.15113_15118delinsTTAAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.596-155_596-150delinsTTAAAA MANE Select	ENSP00000384957.2:n.596-155_596-150delins...
ENST00000264692.8:c.434-155_434-150delinsTTAAAA	ENSP00000264692.5:n.434-155_434-150delins...
ENST00000403665.6:c.596-155_596-150delinsTTAAAA	ENSP00000384957.2:n.596-155_596-150delins...
ENST00000452239.1:c.43-155_43-150delinsTTAAAA
NM_000128.3:c.596-155_596-150delinsTTAAAA , LRG_583t1:c.596-155_596-150delinsTTAAAA	NP_000119.1:n.596-155_596-150delinsTTAAAA...
XM_005262821.2:c.596-155_596-150delinsTTAAAA	XP_005262878.1:n.596-155_596-150delinsTTA...
XM_005262822.2:c.596-155_596-150delinsTTAAAA	XP_005262879.1:n.596-155_596-150delinsTTA...
XM_005262823.2:c.485+1801_485+1806delinsTTAAAA	XP_005262880.1:n.485+1801_485+1806delinsT...
XM_005262824.1:c.596-155_596-150delinsTTAAAA	XP_005262881.1:n.596-155_596-150delinsTTA...
XM_006714137.1:c.596-155_596-150delinsTTAAAA	XP_006714200.1:n.596-155_596-150delinsTTA...
XR_938706.1:n.948-155_948-150delinsTTAAAA
XR_938707.1:n.948-155_948-150delinsTTAAAA
XM_005262821.4:c.596-155_596-150delinsTTAAAA	XP_005262878.1:n.596-155_596-150delinsTTA...
XM_005262822.4:c.596-155_596-150delinsTTAAAA	XP_005262879.1:n.596-155_596-150delinsTTA...
XM_005262823.4:c.485+1801_485+1806delinsTTAAAA	XP_005262880.1:n.485+1801_485+1806delinsT...
XM_006714137.3:c.596-155_596-150delinsTTAAAA	XP_006714200.1:n.596-155_596-150delinsTTA...
XM_017007884.2:c.596-155_596-150delinsTTAAAA	XP_016863373.1:n.596-155_596-150delinsTTA...
XM_017007885.2:c.596-155_596-150delinsTTAAAA	XP_016863374.1:n.596-155_596-150delinsTTA...
XM_017007886.2:c.596-155_596-150delinsTTAAAA	XP_016863375.1:n.596-155_596-150delinsTTA...
XR_001741172.2:n.929-155_929-150delinsTTAAAA
NM_000128.4:c.596-155_596-150delinsTTAAAA MANE Select	NP_000119.1:n.596-155_596-150delinsTTAAAA...