Canonical Allele Identifier: CA358943712

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187206958A>G (hg19) ; chr4:g.186285804A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285804A>G , CM000666.2:g.186285804A>G	GRCh38
NC_000004.11:g.187206958A>G , CM000666.1:g.187206958A>G	GRCh37
NC_000004.10:g.187443952A>G	NCBI36
NG_008051.1:g.24841A>G , LRG_583:g.24841A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1471A>G MANE Select	ENSP00000384957.2:p.Asn491Asp
ENST00000264691.4:c.167A>G
ENST00000264692.8:c.1309A>G	ENSP00000264692.5:p.Asn437Asp
ENST00000403665.6:c.1471A>G	ENSP00000384957.2:p.Asn491Asp
NM_000128.3:c.1471A>G , LRG_583t1:c.1471A>G	NP_000119.1:p.Asn491Asp
XM_005262821.2:c.1474A>G	XP_005262878.1:p.Asn492Asp
XM_005262822.2:c.1474A>G	XP_005262879.1:p.Asn492Asp
XM_005262823.2:c.1204A>G	XP_005262880.1:p.Asn402Asp
XM_005262824.1:c.1474A>G	XP_005262881.1:p.Asn492Asp
XM_006714137.1:c.1426A>G	XP_006714200.1:p.Asn476Asp
XR_938706.1:n.1879A>G
XR_938707.1:n.1879A>G
XM_005262821.4:c.1474A>G	XP_005262878.1:p.Asn492Asp
XM_005262822.4:c.1474A>G	XP_005262879.1:p.Asn492Asp
XM_005262823.4:c.1204A>G	XP_005262880.1:p.Asn402Asp
XM_006714137.3:c.1426A>G	XP_006714200.1:p.Asn476Asp
XR_001741172.2:n.1945A>G
NM_000128.4:c.1471A>G MANE Select	NP_000119.1:p.Asn491Asp