Canonical Allele Identifier: CA3164145

Linked Data

dbSNP Id: rs758865890

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186288592T>C , CM000666.2:g.186288592T>C GRCh38
NC_000004.11:g.187209746T>C , CM000666.1:g.187209746T>C GRCh37
NC_000004.10:g.187446740T>C NCBI36
NG_008051.1:g.27629T>C , LRG_583:g.27629T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1856T>C (F11) MANE Select ENSP00000384957.2:p.Leu619Pro
ENST00000264691.4:c.456T>C (F11)
ENST00000264692.8:c.1694T>C (F11) ENSP00000264692.5:p.Leu565Pro
ENST00000403665.6:c.1856T>C (F11) ENSP00000384957.2:p.Leu619Pro
ENST00000503841.1:n.375T>C (F11)
NM_000128.3:c.1856T>C , LRG_583t1:c.1856T>C (F11) NP_000119.1:p.Leu619Pro
NR_033900.1:n.902A>G (F11-AS1)
XM_005262821.2:c.1859T>C (F11) XP_005262878.1:p.Leu620Pro
XM_005262822.2:c.1763T>C (F11) XP_005262879.1:p.Leu588Pro
XM_005262823.2:c.1589T>C (F11) XP_005262880.1:p.Leu530Pro
XM_006714137.1:c.1811T>C (F11) XP_006714200.1:p.Leu604Pro
XM_005262821.4:c.1859T>C (F11) XP_005262878.1:p.Leu620Pro
XM_005262822.4:c.1763T>C (F11) XP_005262879.1:p.Leu588Pro
XM_005262823.4:c.1589T>C (F11) XP_005262880.1:p.Leu530Pro
XM_006714137.3:c.1811T>C (F11) XP_006714200.1:p.Leu604Pro
NM_000128.4:c.1856T>C (F11) MANE Select NP_000119.1:p.Leu619Pro