Canonical Allele Identifier: CA358942128
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284223A>C , CM000666.2:g.186284223A>C GRCh38
NC_000004.11:g.187205377A>C , CM000666.1:g.187205377A>C GRCh37
NC_000004.10:g.187442371A>C NCBI36
NG_008051.1:g.23260A>C , LRG_583:g.23260A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1267A>C MANE Select ENSP00000384957.2:p.Asn423His
ENST00000264692.8:c.1105A>C ENSP00000264692.5:p.Asn369His
ENST00000403665.6:c.1267A>C ENSP00000384957.2:p.Asn423His
NM_000128.3:c.1267A>C , LRG_583t1:c.1267A>C NP_000119.1:p.Asn423His
XM_005262821.2:c.1270A>C XP_005262878.1:p.Asn424His
XM_005262822.2:c.1270A>C XP_005262879.1:p.Asn424His
XM_005262823.2:c.1000A>C XP_005262880.1:p.Asn334His
XM_005262824.1:c.1270A>C XP_005262881.1:p.Asn424His
XM_006714137.1:c.1222A>C XP_006714200.1:p.Asn408His
XR_938706.1:n.1675A>C
XR_938707.1:n.1675A>C
XM_005262821.4:c.1270A>C XP_005262878.1:p.Asn424His
XM_005262822.4:c.1270A>C XP_005262879.1:p.Asn424His
XM_005262823.4:c.1000A>C XP_005262880.1:p.Asn334His
XM_006714137.3:c.1222A>C XP_006714200.1:p.Asn408His
XR_001741172.2:n.1741A>C
NM_000128.4:c.1267A>C MANE Select NP_000119.1:p.Asn423His