Canonical Allele Identifier: CA358942324

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205410T>A (hg19) ; chr4:g.186284256T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284256T>A , CM000666.2:g.186284256T>A	GRCh38
NC_000004.11:g.187205410T>A , CM000666.1:g.187205410T>A	GRCh37
NC_000004.10:g.187442404T>A	NCBI36
NG_008051.1:g.23293T>A , LRG_583:g.23293T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1300T>A MANE Select	ENSP00000384957.2:p.Tyr434Asn
ENST00000264692.8:c.1138T>A	ENSP00000264692.5:p.Tyr380Asn
ENST00000403665.6:c.1300T>A	ENSP00000384957.2:p.Tyr434Asn
NM_000128.3:c.1300T>A , LRG_583t1:c.1300T>A	NP_000119.1:p.Tyr434Asn
XM_005262821.2:c.1303T>A	XP_005262878.1:p.Tyr435Asn
XM_005262822.2:c.1303T>A	XP_005262879.1:p.Tyr435Asn
XM_005262823.2:c.1033T>A	XP_005262880.1:p.Tyr345Asn
XM_005262824.1:c.1303T>A	XP_005262881.1:p.Tyr435Asn
XM_006714137.1:c.1255T>A	XP_006714200.1:p.Tyr419Asn
XR_938706.1:n.1708T>A
XR_938707.1:n.1708T>A
XM_005262821.4:c.1303T>A	XP_005262878.1:p.Tyr435Asn
XM_005262822.4:c.1303T>A	XP_005262879.1:p.Tyr435Asn
XM_005262823.4:c.1033T>A	XP_005262880.1:p.Tyr345Asn
XM_006714137.3:c.1255T>A	XP_006714200.1:p.Tyr419Asn
XR_001741172.2:n.1774T>A
NM_000128.4:c.1300T>A MANE Select	NP_000119.1:p.Tyr434Asn