Canonical Allele Identifier: CA5455785
Gene: SVIL HGNC NCBI
SVIL-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29458292G>A , CM000672.2:g.29458292G>A GRCh38
NC_000010.10:g.29747221G>A , CM000672.1:g.29747221G>A GRCh37
NC_000010.9:g.29787227G>A NCBI36
NG_033998.1:g.282510C>T

Transcript Alleles

HGVS Amino-acid Change
NM_021738.3:c.6600C>T (SVIL) MANE Select NP_068506.2:p.Pro2200=
ENST00000355867.9:c.6600C>T (SVIL) MANE Select ENSP00000348128.4:p.Pro2200=
NM_001323599.1:c.5670C>T (SVIL) NP_001310528.1:p.Pro1890=
NM_001323599.2:c.5670C>T (SVIL) NP_001310528.1:p.Pro1890=
NM_001323600.1:c.5418C>T (SVIL) NP_001310529.1:p.Pro1806=
NM_003174.3:c.5322C>T (SVIL) NP_003165.2:p.Pro1774=
NM_021738.2:c.6600C>T (SVIL) NP_068506.2:p.Pro2200=
NR_110920.1:n.225G>A (SVIL-AS1)
NR_110921.1:n.207-24541G>A (SVIL-AS1)
NR_110922.1:n.182-24541G>A (SVIL-AS1)
NR_110925.1:n.207-8948G>A (SVIL-AS1)
NR_110926.1:n.182-8948G>A (SVIL-AS1)
NR_110927.1:n.182-28863G>A (SVIL-AS1)
NR_110928.1:n.276-10628G>A (SVIL-AS1)
NR_110929.1:n.182-10628G>A (SVIL-AS1)
ENST00000355867.8:c.6600C>T (SVIL) ENSP00000348128.4:p.Pro2200=
ENST00000375398.6:c.6504C>T (SVIL) ENSP00000364547.3:p.Pro2168=
ENST00000375400.7:c.5322C>T (SVIL) ENSP00000364549.3:p.Pro1774=
ENST00000413405.5:n.177-28863G>A (SVIL-AS1)
ENST00000413405.6:n.182-28863G>A (SVIL-AS1)
ENST00000414457.5:n.158-24541G>A (SVIL-AS1)
ENST00000414457.6:n.207-24541G>A (SVIL-AS1)
ENST00000423223.5:n.155-24541G>A (SVIL-AS1)
ENST00000423223.6:n.182-24541G>A (SVIL-AS1)
ENST00000430295.5:n.332G>A (SVIL-AS1)
ENST00000438202.5:n.157G>A (SVIL-AS1)
ENST00000445521.5:n.150-8948G>A (SVIL-AS1)
ENST00000445521.6:n.184-8948G>A (SVIL-AS1)
ENST00000446807.5:n.179G>A (SVIL-AS1)
ENST00000455774.1:n.276-10628G>A (SVIL-AS1)
ENST00000646086.2:n.207-28863G>A (SVIL-AS1)
ENST00000674475.1:c.5670C>T (SVIL) ENSP00000501521.1:p.Pro1890=
ENST00000684815.1:n.236+42880G>A (SVIL-AS1)
ENST00000686070.1:n.225G>A (SVIL-AS1)
ENST00000686207.1:n.159-8948G>A (SVIL-AS1)
ENST00000687838.1:n.184-34671G>A (SVIL-AS1)
XM_005252570.2:c.6726C>T (SVIL) XP_005252627.1:p.Pro2242=
XM_005252571.2:c.6726C>T (SVIL) XP_005252628.1:p.Pro2242=
XM_005252571.4:c.6726C>T (SVIL) XP_005252628.1:p.Pro2242=
XM_005252573.2:c.6726C>T (SVIL) XP_005252630.1:p.Pro2242=
XM_005252573.3:c.6726C>T (SVIL) XP_005252630.1:p.Pro2242=
XM_011519630.1:c.6648C>T (SVIL) XP_011517932.1:p.Pro2216=
XM_011519631.1:c.6630C>T (SVIL) XP_011517933.1:p.Pro2210=
XM_011519632.1:c.6555C>T (SVIL) XP_011517934.1:p.Pro2185=
XM_011519633.1:c.6504C>T (SVIL) XP_011517935.1:p.Pro2168=
XM_011519634.1:c.6726C>T (SVIL) XP_011517936.1:p.Pro2242=
XM_011519635.1:c.6726C>T (SVIL) XP_011517937.1:p.Pro2242=
XM_011519635.2:c.6726C>T (SVIL) XP_011517937.1:p.Pro2242=
XM_011519636.1:c.5796C>T (SVIL) XP_011517938.1:p.Pro1932=
XM_011519637.1:c.5544C>T (SVIL) XP_011517939.1:p.Pro1848=
XM_011519638.1:c.5448C>T (SVIL) XP_011517940.1:p.Pro1816=
XM_024448138.1:c.6960C>T (SVIL) XP_024303906.1:p.Pro2320=
XM_024448139.1:c.6648C>T (SVIL) XP_024303907.1:p.Pro2216=
XM_024448140.1:c.6645C>T (SVIL) XP_024303908.1:p.Pro2215=
XM_024448141.1:c.6630C>T (SVIL) XP_024303909.1:p.Pro2210=
XM_024448142.1:c.6555C>T (SVIL) XP_024303910.1:p.Pro2185=
XM_024448143.1:c.6504C>T (SVIL) XP_024303911.1:p.Pro2168=
XM_024448144.1:c.5796C>T (SVIL) XP_024303912.1:p.Pro1932=
XM_024448145.1:c.5700C>T (SVIL) XP_024303913.1:p.Pro1900=
XM_024448146.1:c.5625C>T (SVIL) XP_024303914.1:p.Pro1875=
XM_024448147.1:c.5544C>T (SVIL) XP_024303915.1:p.Pro1848=
XM_024448148.1:c.5448C>T (SVIL) XP_024303916.1:p.Pro1816=