Canonical Allele Identifier: CA112103720

Gene: F11

Linked Data

• dbSNP Id: rs267600113
• MyVariant Identifiers: chr4:g.187206856G>A (hg19) ; chr4:g.186285702G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285702G>A , CM000666.2:g.186285702G>A	GRCh38
NC_000004.11:g.187206856G>A , CM000666.1:g.187206856G>A	GRCh37
NC_000004.10:g.187443850G>A	NCBI36
NG_008051.1:g.24739G>A , LRG_583:g.24739G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1369G>A MANE Select	ENSP00000384957.2:p.Asp457Asn
ENST00000264691.4:c.65G>A
ENST00000264692.8:c.1207G>A	ENSP00000264692.5:p.Asp403Asn
ENST00000403665.6:c.1369G>A	ENSP00000384957.2:p.Asp457Asn
NM_000128.3:c.1369G>A , LRG_583t1:c.1369G>A	NP_000119.1:p.Asp457Asn
XM_005262821.2:c.1372G>A	XP_005262878.1:p.Asp458Asn
XM_005262822.2:c.1372G>A	XP_005262879.1:p.Asp458Asn
XM_005262823.2:c.1102G>A	XP_005262880.1:p.Asp368Asn
XM_005262824.1:c.1372G>A	XP_005262881.1:p.Asp458Asn
XM_006714137.1:c.1324G>A	XP_006714200.1:p.Asp442Asn
XR_938706.1:n.1777G>A
XR_938707.1:n.1777G>A
XM_005262821.4:c.1372G>A	XP_005262878.1:p.Asp458Asn
XM_005262822.4:c.1372G>A	XP_005262879.1:p.Asp458Asn
XM_005262823.4:c.1102G>A	XP_005262880.1:p.Asp368Asn
XM_006714137.3:c.1324G>A	XP_006714200.1:p.Asp442Asn
XR_001741172.2:n.1843G>A
NM_000128.4:c.1369G>A MANE Select	NP_000119.1:p.Asp457Asn