Canonical Allele Identifier: CA3344538
Community Standard Title: NM_032290.4(SLF1):c.1528A>G (p.Ile510Val)
Gene: SLF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.94666020A>G , CM000667.2:g.94666020A>G GRCh38
NC_000005.9:g.94001725A>G , CM000667.1:g.94001725A>G GRCh37
NC_000005.8:g.94027481A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_032290.4:c.1528A>G MANE Select NP_115666.2:p.Ile510Val
ENST00000265140.10:c.1528A>G MANE Select ENSP00000265140.5:p.Ile510Val
NM_032290.3:c.1528A>G NP_115666.2:p.Ile510Val
ENST00000265140.9:c.1528A>G ENSP00000265140.5:p.Ile510Val
XM_005272113.3:c.1528A>G XP_005272170.1:p.Ile510Val
XM_006714720.2:c.151A>G XP_006714783.1:p.Ile51Val
XM_011543682.1:c.1528A>G XP_011541984.1:p.Ile510Val
XM_011543683.1:c.1528A>G XP_011541985.1:p.Ile510Val
XM_011543684.1:c.1528A>G XP_011541986.1:p.Ile510Val
XM_011543685.1:c.1528A>G XP_011541987.1:p.Ile510Val
XM_011543686.1:c.1528A>G XP_011541988.1:p.Ile510Val
XM_011543687.1:c.1528A>G XP_011541989.1:p.Ile510Val
XM_011543688.1:c.1528A>G XP_011541990.1:p.Ile510Val
XM_011543689.1:c.1528A>G XP_011541991.1:p.Ile510Val
XM_017009979.2:c.1528A>G XP_016865468.1:p.Ile510Val
XM_017009981.2:c.1528A>G XP_016865470.1:p.Ile510Val
XM_017009983.1:c.151A>G XP_016865472.1:p.Ile51Val
XM_017009984.1:c.151A>G XP_016865473.1:p.Ile51Val
XM_024446231.1:c.1528A>G XP_024301999.1:p.Ile510Val
XM_024446232.1:c.1528A>G XP_024302000.1:p.Ile510Val
XM_024446233.1:c.1528A>G XP_024302001.1:p.Ile510Val
XM_024446234.1:c.1528A>G XP_024302002.1:p.Ile510Val
XM_024446235.1:c.1378A>G XP_024302003.1:p.Ile460Val
XM_024446236.1:c.1528A>G XP_024302004.1:p.Ile510Val
XM_024446237.1:c.1528A>G XP_024302005.1:p.Ile510Val
XM_024446238.1:c.*57A>G XP_024302006.1:n.*57A>G
XM_024446239.1:c.*57A>G XP_024302007.1:n.*57A>G