Canonical Allele Identifier: CA358941983

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205345A>T (hg19) ; chr4:g.186284191A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284191A>T , CM000666.2:g.186284191A>T	GRCh38
NC_000004.11:g.187205345A>T , CM000666.1:g.187205345A>T	GRCh37
NC_000004.10:g.187442339A>T	NCBI36
NG_008051.1:g.23228A>T , LRG_583:g.23228A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1235A>T MANE Select	ENSP00000384957.2:p.Gln412Leu
ENST00000264692.8:c.1073A>T	ENSP00000264692.5:p.Gln358Leu
ENST00000403665.6:c.1235A>T	ENSP00000384957.2:p.Gln412Leu
NM_000128.3:c.1235A>T , LRG_583t1:c.1235A>T	NP_000119.1:p.Gln412Leu
XM_005262821.2:c.1238A>T	XP_005262878.1:p.Gln413Leu
XM_005262822.2:c.1238A>T	XP_005262879.1:p.Gln413Leu
XM_005262823.2:c.968A>T	XP_005262880.1:p.Gln323Leu
XM_005262824.1:c.1238A>T	XP_005262881.1:p.Gln413Leu
XM_006714137.1:c.1190A>T	XP_006714200.1:p.Gln397Leu
XR_938706.1:n.1643A>T
XR_938707.1:n.1643A>T
XM_005262821.4:c.1238A>T	XP_005262878.1:p.Gln413Leu
XM_005262822.4:c.1238A>T	XP_005262879.1:p.Gln413Leu
XM_005262823.4:c.968A>T	XP_005262880.1:p.Gln323Leu
XM_006714137.3:c.1190A>T	XP_006714200.1:p.Gln397Leu
XR_001741172.2:n.1709A>T
NM_000128.4:c.1235A>T MANE Select	NP_000119.1:p.Gln412Leu