Canonical Allele Identifier: CA358941898

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205328C>A (hg19) ; chr4:g.186284174C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284174C>A , CM000666.2:g.186284174C>A	GRCh38
NC_000004.11:g.187205328C>A , CM000666.1:g.187205328C>A	GRCh37
NC_000004.10:g.187442322C>A	NCBI36
NG_008051.1:g.23211C>A , LRG_583:g.23211C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1218C>A MANE Select	ENSP00000384957.2:p.His406Gln
ENST00000264692.8:c.1056C>A	ENSP00000264692.5:p.His352Gln
ENST00000403665.6:c.1218C>A	ENSP00000384957.2:p.His406Gln
NM_000128.3:c.1218C>A , LRG_583t1:c.1218C>A	NP_000119.1:p.His406Gln
XM_005262821.2:c.1221C>A	XP_005262878.1:p.His407Gln
XM_005262822.2:c.1221C>A	XP_005262879.1:p.His407Gln
XM_005262823.2:c.951C>A	XP_005262880.1:p.His317Gln
XM_005262824.1:c.1221C>A	XP_005262881.1:p.His407Gln
XM_006714137.1:c.1173C>A	XP_006714200.1:p.His391Gln
XR_938706.1:n.1626C>A
XR_938707.1:n.1626C>A
XM_005262821.4:c.1221C>A	XP_005262878.1:p.His407Gln
XM_005262822.4:c.1221C>A	XP_005262879.1:p.His407Gln
XM_005262823.4:c.951C>A	XP_005262880.1:p.His317Gln
XM_006714137.3:c.1173C>A	XP_006714200.1:p.His391Gln
XM_017007884.2:c.*2190C>A	XP_016863373.1:n.*2190C>A
XR_001741172.2:n.1692C>A
NM_000128.4:c.1218C>A MANE Select	NP_000119.1:p.His406Gln