Canonical Allele Identifier: CA358943493

Gene: F11

Linked Data

• dbSNP Id: rs1305611614
• gnomAD v2: 4-187206906-A-T
• gnomAD v4: 4-186285752-A-T
• MyVariant Identifiers: chr4:g.187206906A>T (hg19) ; chr4:g.186285752A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285752A>T , CM000666.2:g.186285752A>T	GRCh38
NC_000004.11:g.187206906A>T , CM000666.1:g.187206906A>T	GRCh37
NC_000004.10:g.187443900A>T	NCBI36
NG_008051.1:g.24789A>T , LRG_583:g.24789A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1419A>T MANE Select	ENSP00000384957.2:p.Lys473Asn
ENST00000264691.4:c.115A>T
ENST00000264692.8:c.1257A>T	ENSP00000264692.5:p.Lys419Asn
ENST00000403665.6:c.1419A>T	ENSP00000384957.2:p.Lys473Asn
NM_000128.3:c.1419A>T , LRG_583t1:c.1419A>T	NP_000119.1:p.Lys473Asn
XM_005262821.2:c.1422A>T	XP_005262878.1:p.Lys474Asn
XM_005262822.2:c.1422A>T	XP_005262879.1:p.Lys474Asn
XM_005262823.2:c.1152A>T	XP_005262880.1:p.Lys384Asn
XM_005262824.1:c.1422A>T	XP_005262881.1:p.Lys474Asn
XM_006714137.1:c.1374A>T	XP_006714200.1:p.Lys458Asn
XR_938706.1:n.1827A>T
XR_938707.1:n.1827A>T
XM_005262821.4:c.1422A>T	XP_005262878.1:p.Lys474Asn
XM_005262822.4:c.1422A>T	XP_005262879.1:p.Lys474Asn
XM_005262823.4:c.1152A>T	XP_005262880.1:p.Lys384Asn
XM_006714137.3:c.1374A>T	XP_006714200.1:p.Lys458Asn
XR_001741172.2:n.1893A>T
NM_000128.4:c.1419A>T MANE Select	NP_000119.1:p.Lys473Asn