Canonical Allele Identifier: CA1630856047
Community Standard Title: NM_020921.4(NIN):c.3331C= (p.Pro1111=)
Gene: NIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50757699G= , CM000676.2:g.50757699G= GRCh38
NC_000014.8:g.51224417G= , CM000676.1:g.51224417G= GRCh37
NC_000014.7:g.50294167G= NCBI36
NG_032968.1:g.78423C=

Transcript Alleles

HGVS Amino-acid Change
NM_020921.4:c.3331C= MANE Select NP_065972.4:p.Pro1111=
ENST00000530997.7:c.3331C= MANE Select ENSP00000436092.2:p.Pro1111=
NM_016350.4:c.2399+2158C= NP_057434.4:n.2399+2158C=
NM_016350.5:c.2399+2158C= NP_057434.4:n.2399+2158C=
NM_020921.3:c.3331C= NP_065972.3:p.Pro1111=
NM_182944.2:c.3331C= NP_891989.2:p.Pro1111=
NM_182944.3:c.3331C= NP_891989.3:p.Pro1111=
NM_182946.1:c.3331C= NP_891991.1:p.Pro1111=
NM_182946.2:c.3331C= NP_891991.2:p.Pro1111=
ENST00000245441.9:c.3331C= ENSP00000245441.5:p.Pro1111=
ENST00000324330.13:c.2399+2158C= ENSP00000324210.10:n.2399+2158C=
ENST00000382041.7:c.3331C= ENSP00000371472.3:p.Pro1111=
ENST00000382043.8:c.2399+2158C= ENSP00000371474.4:n.2399+2158C=
ENST00000389869.7:c.1802C=
ENST00000453196.5:c.3331C= ENSP00000412391.1:p.Pro1111=
ENST00000453196.6:c.3331C= ENSP00000412391.1:p.Pro1111=
ENST00000476352.5:c.3331C= ENSP00000432924.1:p.Pro1111=
ENST00000485005.2:c.2399+2158C= ENSP00000431485.2:n.2399+2158C=
ENST00000530853.5:c.1802C=
ENST00000530997.6:c.3331C= ENSP00000436092.2:p.Pro1111=
ENST00000673657.1:c.*1203+2158C= ENSP00000501199.1:n.*1203+2158C=
ENST00000674030.1:c.*666+2158C= ENSP00000501260.1:n.*666+2158C=
ENST00000706705.1:c.1733+2158C= ENSP00000516508.1:n.1733+2158C=
ENST00000706706.1:c.2399+2158C= ENSP00000516509.1:n.2399+2158C=
XM_005267735.3:c.2399+2158C= XP_005267792.1:n.2399+2158C=
XM_006720160.2:c.3331C= XP_006720223.2:p.Pro1111=
XM_011536817.1:c.3421C= XP_011535119.1:p.Pro1141=
XM_011536818.1:c.3331C= XP_011535120.1:p.Pro1111=
XM_011536819.1:c.3421C= XP_011535121.1:p.Pro1141=
XM_011536819.3:c.3421C= XP_011535121.1:p.Pro1141=
XM_011536820.1:c.3421C= XP_011535122.1:p.Pro1141=
XM_011536821.1:c.2665C= XP_011535123.1:p.Pro889=
XM_011536822.1:c.2489+2158C= XP_011535124.1:n.2489+2158C=
XM_011536822.2:c.2489+2158C= XP_011535124.1:n.2489+2158C=
XM_011536823.1:c.3349C= XP_011535125.1:p.Pro1117=
XM_011536823.2:c.3349C= XP_011535125.1:p.Pro1117=
XM_011536824.1:c.2399+2158C= XP_011535126.1:n.2399+2158C=
XM_024449622.1:c.3421C= XP_024305390.1:p.Pro1141=
XR_001750344.2:n.3619C=
XR_001750345.2:n.3619C=
XR_001750346.2:n.3541C=
XR_001750347.2:n.2681+2158C=
XR_001750348.2:n.2681+2158C=
XR_001750349.2:n.2609+2158C=
XR_001750350.2:n.2609+2158C=