Canonical Allele Identifier: CA358941617

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205273T>A (hg19) ; chr4:g.186284119T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284119T>A , CM000666.2:g.186284119T>A	GRCh38
NC_000004.11:g.187205273T>A , CM000666.1:g.187205273T>A	GRCh37
NC_000004.10:g.187442267T>A	NCBI36
NG_008051.1:g.23156T>A , LRG_583:g.23156T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1163T>A MANE Select	ENSP00000384957.2:p.Ile388Asn
ENST00000264692.8:c.1001T>A	ENSP00000264692.5:p.Ile334Asn
ENST00000403665.6:c.1163T>A	ENSP00000384957.2:p.Ile388Asn
NM_000128.3:c.1163T>A , LRG_583t1:c.1163T>A	NP_000119.1:p.Ile388Asn
XM_005262821.2:c.1166T>A	XP_005262878.1:p.Ile389Asn
XM_005262822.2:c.1166T>A	XP_005262879.1:p.Ile389Asn
XM_005262823.2:c.896T>A	XP_005262880.1:p.Ile299Asn
XM_005262824.1:c.1166T>A	XP_005262881.1:p.Ile389Asn
XM_006714137.1:c.1118T>A	XP_006714200.1:p.Ile373Asn
XR_938706.1:n.1571T>A
XR_938707.1:n.1571T>A
XM_005262821.4:c.1166T>A	XP_005262878.1:p.Ile389Asn
XM_005262822.4:c.1166T>A	XP_005262879.1:p.Ile389Asn
XM_005262823.4:c.896T>A	XP_005262880.1:p.Ile299Asn
XM_006714137.3:c.1118T>A	XP_006714200.1:p.Ile373Asn
XM_017007884.2:c.*2135T>A	XP_016863373.1:n.*2135T>A
XM_017007885.2:c.*31T>A	XP_016863374.1:n.*31T>A
XR_001741172.2:n.1637T>A
NM_000128.4:c.1163T>A MANE Select	NP_000119.1:p.Ile388Asn