Canonical Allele Identifier: CA358938205
Gene: F11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280343T>C , CM000666.2:g.186280343T>C GRCh38
NC_000004.11:g.187201497T>C , CM000666.1:g.187201497T>C GRCh37
NC_000004.10:g.187438491T>C NCBI36
NG_008051.1:g.19380T>C , LRG_583:g.19380T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.986T>C MANE Select ENSP00000384957.2:p.Phe329Ser
ENST00000264692.8:c.824T>C ENSP00000264692.5:p.Phe275Ser
ENST00000403665.6:c.986T>C ENSP00000384957.2:p.Phe329Ser
ENST00000452239.1:c.433T>C
NM_000128.3:c.986T>C , LRG_583t1:c.986T>C NP_000119.1:p.Phe329Ser
XM_005262821.2:c.986T>C XP_005262878.1:p.Phe329Ser
XM_005262822.2:c.986T>C XP_005262879.1:p.Phe329Ser
XM_005262823.2:c.716T>C XP_005262880.1:p.Phe239Ser
XM_005262824.1:c.986T>C XP_005262881.1:p.Phe329Ser
XM_006714137.1:c.938T>C XP_006714200.1:p.Phe313Ser
XR_938706.1:n.1338T>C
XR_938707.1:n.1338T>C
XM_005262821.4:c.986T>C XP_005262878.1:p.Phe329Ser
XM_005262822.4:c.986T>C XP_005262879.1:p.Phe329Ser
XM_005262823.4:c.716T>C XP_005262880.1:p.Phe239Ser
XM_006714137.3:c.938T>C XP_006714200.1:p.Phe313Ser
XM_017007884.2:c.986T>C XP_016863373.1:p.Phe329Ser
XM_017007885.2:c.986T>C XP_016863374.1:p.Phe329Ser
XM_017007886.2:c.986T>C XP_016863375.1:p.Phe329Ser
XR_001741172.2:n.1319T>C
NM_000128.4:c.986T>C MANE Select NP_000119.1:p.Phe329Ser