Canonical Allele Identifier: CA358945734

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287813A>G , CM000666.2:g.186287813A>G GRCh38
NC_000004.11:g.187208967A>G , CM000666.1:g.187208967A>G GRCh37
NC_000004.10:g.187445961A>G NCBI36
NG_008051.1:g.26850A>G , LRG_583:g.26850A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1706A>G (F11) MANE Select ENSP00000384957.2:p.Asp569Gly
ENST00000264691.4:c.306A>G (F11)
ENST00000264692.8:c.1544A>G (F11) ENSP00000264692.5:p.Asp515Gly
ENST00000403665.6:c.1706A>G (F11) ENSP00000384957.2:p.Asp569Gly
ENST00000503841.1:n.225A>G (F11)
NM_000128.3:c.1706A>G , LRG_583t1:c.1706A>G (F11) NP_000119.1:p.Asp569Gly
NR_033900.1:n.1066+615T>C (F11-AS1)
XM_005262821.2:c.1709A>G (F11) XP_005262878.1:p.Asp570Gly
XM_005262822.2:c.1613A>G (F11) XP_005262879.1:p.Asp538Gly
XM_005262823.2:c.1439A>G (F11) XP_005262880.1:p.Asp480Gly
XM_006714137.1:c.1661A>G (F11) XP_006714200.1:p.Asp554Gly
XM_005262821.4:c.1709A>G (F11) XP_005262878.1:p.Asp570Gly
XM_005262822.4:c.1613A>G (F11) XP_005262879.1:p.Asp538Gly
XM_005262823.4:c.1439A>G (F11) XP_005262880.1:p.Asp480Gly
XM_006714137.3:c.1661A>G (F11) XP_006714200.1:p.Asp554Gly
NM_000128.4:c.1706A>G (F11) MANE Select NP_000119.1:p.Asp569Gly