Canonical Allele Identifier: CA442639202

Gene: F11

Linked Data

• gnomAD v4: 4-186285650-T-A
• MyVariant Identifiers: chr4:g.187206804T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285650T>A , CM000666.2:g.186285650T>A	GRCh38
NC_000004.11:g.187206804T>A , CM000666.1:g.187206804T>A	GRCh37
NC_000004.10:g.187443798T>A	NCBI36
NG_008051.1:g.24687T>A , LRG_583:g.24687T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1317T>A MANE Select	ENSP00000384957.2:p.Pro439=
ENST00000264691.4:c.13T>A
ENST00000264692.8:c.1155T>A	ENSP00000264692.5:p.Pro385=
ENST00000403665.6:c.1317T>A	ENSP00000384957.2:p.Pro439=
NM_000128.3:c.1317T>A , LRG_583t1:c.1317T>A	NP_000119.1:p.Pro439=
XM_005262821.2:c.1320T>A	XP_005262878.1:p.Pro440=
XM_005262822.2:c.1320T>A	XP_005262879.1:p.Pro440=
XM_005262823.2:c.1050T>A	XP_005262880.1:p.Pro350=
XM_005262824.1:c.1320T>A	XP_005262881.1:p.Pro440=
XM_006714137.1:c.1272T>A	XP_006714200.1:p.Pro424=
XR_938706.1:n.1725T>A
XR_938707.1:n.1725T>A
XM_005262821.4:c.1320T>A	XP_005262878.1:p.Pro440=
XM_005262822.4:c.1320T>A	XP_005262879.1:p.Pro440=
XM_005262823.4:c.1050T>A	XP_005262880.1:p.Pro350=
XM_006714137.3:c.1272T>A	XP_006714200.1:p.Pro424=
XR_001741172.2:n.1791T>A
NM_000128.4:c.1317T>A MANE Select	NP_000119.1:p.Pro439=