Canonical Allele Identifier: CA7372329
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 540059
dbSNP Id: rs150714865

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104703345C>T , CM000676.2:g.104703345C>T GRCh38
NC_000014.8:g.105169682C>T , CM000676.1:g.105169682C>T GRCh37
NC_000014.7:g.104240727C>T NCBI36
NG_027684.1:g.18740C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392634.9:c.558C>T MANE Select ENSP00000376410.4:p.Ser186=
ENST00000617571.5:c.558C>T ENSP00000483829.2:p.Ser186=
ENST00000674520.1:c.558C>T ENSP00000502593.1:p.Ser186=
ENST00000674662.1:c.558C>T ENSP00000501895.1:p.Ser186=
ENST00000674757.1:c.558C>T ENSP00000502202.1:p.Ser186=
ENST00000674822.1:c.442C>T ENSP00000501552.1:p.Arg148Trp
ENST00000674846.1:c.558C>T ENSP00000502431.1:p.Ser186=
ENST00000674857.1:c.547C>T ENSP00000501687.1:p.Arg183Trp
ENST00000674960.1:c.558C>T ENSP00000501841.1:p.Ser186=
ENST00000674991.1:c.558C>T ENSP00000502004.1:p.Ser186=
ENST00000674994.1:c.558C>T ENSP00000502442.1:p.Ser186=
ENST00000675029.1:n.760C>T
ENST00000675207.1:c.654C>T ENSP00000502644.1:p.Ser218=
ENST00000675329.1:c.558C>T ENSP00000502287.1:p.Ser186=
ENST00000675481.1:c.558C>T ENSP00000502723.1:p.Ser186=
ENST00000675583.1:c.558C>T ENSP00000501740.1:p.Ser186=
ENST00000675638.1:c.558C>T ENSP00000501647.1:p.Ser186=
ENST00000675724.1:c.558C>T ENSP00000502576.1:p.Ser186=
ENST00000675771.1:c.558C>T ENSP00000502104.1:p.Ser186=
ENST00000675797.1:c.558C>T ENSP00000502023.1:p.Ser186=
ENST00000675809.1:c.558C>T ENSP00000502587.1:p.Ser186=
ENST00000675930.1:c.558C>T ENSP00000502456.1:p.Ser186=
ENST00000675980.1:c.558C>T ENSP00000502520.1:p.Ser186=
ENST00000676016.1:c.558C>T ENSP00000502412.1:p.Ser186=
ENST00000676366.1:c.558C>T ENSP00000501605.1:p.Ser186=
ENST00000330634.11:c.558C>T ENSP00000376406.3:p.Ser186=
ENST00000392634.8:c.558C>T ENSP00000376410.4:p.Ser186=
ENST00000398337.8:c.558C>T ENSP00000381380.4:p.Ser186=
NM_001031714.3:c.558C>T NP_001026884.3:p.Ser186=
NM_022489.3:c.558C>T NP_071934.3:p.Ser186=
NM_032714.2:c.558C>T NP_116103.1:p.Ser186=
XM_005268004.3:c.654C>T XP_005268061.1:p.Ser218=
XM_005268005.3:c.654C>T XP_005268062.1:p.Ser218=
XR_943507.1:n.783C>T
XM_005268004.4:c.654C>T XP_005268061.1:p.Ser218=
XM_005268005.4:c.654C>T XP_005268062.1:p.Ser218=
XM_017021595.1:c.654C>T XP_016877084.1:p.Ser218=
XR_001750518.1:n.759C>T
NM_001031714.4:c.558C>T NP_001026884.3:p.Ser186=
NM_022489.4:c.558C>T MANE Select NP_071934.3:p.Ser186=
NM_032714.3:c.558C>T NP_116103.1:p.Ser186=