Canonical Allele Identifier: CA358941970

Gene: F11

Linked Data

• dbSNP Id: rs1741005816
• gnomAD v3: 4-186284188-C-T
• gnomAD v4: 4-186284188-C-T
• MyVariant Identifiers: chr4:g.187205342C>T (hg19) ; chr4:g.186284188C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284188C>T , CM000666.2:g.186284188C>T	GRCh38
NC_000004.11:g.187205342C>T , CM000666.1:g.187205342C>T	GRCh37
NC_000004.10:g.187442336C>T	NCBI36
NG_008051.1:g.23225C>T , LRG_583:g.23225C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1232C>T MANE Select	ENSP00000384957.2:p.Thr411Ile
ENST00000264692.8:c.1070C>T	ENSP00000264692.5:p.Thr357Ile
ENST00000403665.6:c.1232C>T	ENSP00000384957.2:p.Thr411Ile
NM_000128.3:c.1232C>T , LRG_583t1:c.1232C>T	NP_000119.1:p.Thr411Ile
XM_005262821.2:c.1235C>T	XP_005262878.1:p.Thr412Ile
XM_005262822.2:c.1235C>T	XP_005262879.1:p.Thr412Ile
XM_005262823.2:c.965C>T	XP_005262880.1:p.Thr322Ile
XM_005262824.1:c.1235C>T	XP_005262881.1:p.Thr412Ile
XM_006714137.1:c.1187C>T	XP_006714200.1:p.Thr396Ile
XR_938706.1:n.1640C>T
XR_938707.1:n.1640C>T
XM_005262821.4:c.1235C>T	XP_005262878.1:p.Thr412Ile
XM_005262822.4:c.1235C>T	XP_005262879.1:p.Thr412Ile
XM_005262823.4:c.965C>T	XP_005262880.1:p.Thr322Ile
XM_006714137.3:c.1187C>T	XP_006714200.1:p.Thr396Ile
XR_001741172.2:n.1706C>T
NM_000128.4:c.1232C>T MANE Select	NP_000119.1:p.Thr411Ile