Canonical Allele Identifier: CA358941622
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284119T>G , CM000666.2:g.186284119T>G GRCh38
NC_000004.11:g.187205273T>G , CM000666.1:g.187205273T>G GRCh37
NC_000004.10:g.187442267T>G NCBI36
NG_008051.1:g.23156T>G , LRG_583:g.23156T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1163T>G MANE Select ENSP00000384957.2:p.Ile388Ser
ENST00000264692.8:c.1001T>G ENSP00000264692.5:p.Ile334Ser
ENST00000403665.6:c.1163T>G ENSP00000384957.2:p.Ile388Ser
NM_000128.3:c.1163T>G , LRG_583t1:c.1163T>G NP_000119.1:p.Ile388Ser
XM_005262821.2:c.1166T>G XP_005262878.1:p.Ile389Ser
XM_005262822.2:c.1166T>G XP_005262879.1:p.Ile389Ser
XM_005262823.2:c.896T>G XP_005262880.1:p.Ile299Ser
XM_005262824.1:c.1166T>G XP_005262881.1:p.Ile389Ser
XM_006714137.1:c.1118T>G XP_006714200.1:p.Ile373Ser
XR_938706.1:n.1571T>G
XR_938707.1:n.1571T>G
XM_005262821.4:c.1166T>G XP_005262878.1:p.Ile389Ser
XM_005262822.4:c.1166T>G XP_005262879.1:p.Ile389Ser
XM_005262823.4:c.896T>G XP_005262880.1:p.Ile299Ser
XM_006714137.3:c.1118T>G XP_006714200.1:p.Ile373Ser
XM_017007884.2:c.*2135T>G XP_016863373.1:n.*2135T>G
XM_017007885.2:c.*31T>G XP_016863374.1:n.*31T>G
XR_001741172.2:n.1637T>G
NM_000128.4:c.1163T>G MANE Select NP_000119.1:p.Ile388Ser