Canonical Allele Identifier: CA8678153
Community Standard Title: NM_015294.6(TRIM37):c.1999C>T (p.Arg667Ter)
Gene: TRIM37 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.59028673G>A , CM000679.2:g.59028673G>A GRCh38
NC_000017.10:g.57106034G>A , CM000679.1:g.57106034G>A GRCh37
NC_000017.9:g.54460816G>A NCBI36
NG_009298.1:g.83233C>T

Transcript Alleles

HGVS Amino-acid Change
NM_015294.6:c.1999C>T MANE Select NP_056109.1:p.Arg667Ter
ENST00000262294.12:c.1999C>T MANE Select ENSP00000262294.7:p.Arg667Ter
NM_001005207.2:c.1999C>T NP_001005207.1:p.Arg667Ter
NM_001005207.4:c.1999C>T NP_001005207.1:p.Arg667Ter
NM_001005207.5:c.1999C>T NP_001005207.1:p.Arg667Ter
NM_001320987.2:c.1897C>T NP_001307916.1:p.Arg633Ter
NM_001320987.3:c.1897C>T NP_001307916.1:p.Arg633Ter
NM_001320988.2:c.1999C>T NP_001307917.1:p.Arg667Ter
NM_001320988.3:c.1999C>T NP_001307917.1:p.Arg667Ter
NM_001320989.2:c.1999C>T NP_001307918.1:p.Arg667Ter
NM_001320989.3:c.1999C>T NP_001307918.1:p.Arg667Ter
NM_001320990.2:c.1633C>T NP_001307919.1:p.Arg545Ter
NM_001320990.3:c.1633C>T NP_001307919.1:p.Arg545Ter
NM_001353082.1:c.1897C>T NP_001340011.1:p.Arg633Ter
NM_001353082.2:c.1897C>T NP_001340011.1:p.Arg633Ter
NM_001353083.1:c.1264C>T NP_001340012.1:p.Arg422Ter
NM_001353083.2:c.1264C>T NP_001340012.1:p.Arg422Ter
NM_001353084.1:c.1999C>T NP_001340013.1:p.Arg667Ter
NM_001353084.2:c.1999C>T NP_001340013.1:p.Arg667Ter
NM_001353085.1:c.1537C>T NP_001340014.1:p.Arg513Ter
NM_001353085.2:c.1537C>T NP_001340014.1:p.Arg513Ter
NM_001353086.1:c.1948C>T NP_001340015.1:p.Arg650Ter
NM_001353086.2:c.1948C>T NP_001340015.1:p.Arg650Ter
NM_015294.3:c.1999C>T NP_056109.1:p.Arg667Ter
NM_015294.5:c.1999C>T NP_056109.1:p.Arg667Ter
NR_148346.1:n.2502C>T
NR_148346.2:n.2418C>T
NR_148347.1:n.2400C>T
NR_148347.2:n.2316C>T
ENST00000262294.11:c.1999C>T ENSP00000262294.7:p.Arg667Ter
ENST00000393065.6:c.1897C>T ENSP00000376784.2:p.Arg633Ter
ENST00000393066.7:c.1999C>T ENSP00000376785.3:p.Arg667Ter
ENST00000577554.5:c.*1871C>T ENSP00000462340.1:n.*1871C>T
XM_005257385.1:c.1999C>T XP_005257442.1:p.Arg667Ter
XM_005257387.1:c.1897C>T XP_005257444.1:p.Arg633Ter
XM_005257389.1:c.1999C>T XP_005257446.1:p.Arg667Ter
XM_005257390.1:c.1999C>T XP_005257447.1:p.Arg667Ter
XM_011524831.1:c.1999C>T XP_011523133.1:p.Arg667Ter
XM_011524832.1:c.1999C>T XP_011523134.1:p.Arg667Ter
XM_011524832.2:c.1999C>T XP_011523134.1:p.Arg667Ter
XM_011524833.1:c.1948C>T XP_011523135.1:p.Arg650Ter
XM_011524834.1:c.1897C>T XP_011523136.1:p.Arg633Ter
XM_011524835.1:c.1999C>T XP_011523137.1:p.Arg667Ter
XM_011524836.1:c.1999C>T XP_011523138.1:p.Arg667Ter
XM_011524837.1:c.1999C>T XP_011523139.1:p.Arg667Ter
XM_017024662.1:c.1999C>T XP_016880151.1:p.Arg667Ter
XM_017024663.2:c.1999C>T XP_016880152.1:p.Arg667Ter
XM_017024664.1:c.1948C>T XP_016880153.1:p.Arg650Ter
XM_017024665.1:c.1897C>T XP_016880154.1:p.Arg633Ter
XM_017024667.1:c.1948C>T XP_016880156.1:p.Arg650Ter
XM_017024669.2:c.1846C>T XP_016880158.1:p.Arg616Ter
XM_017024670.2:c.1897C>T XP_016880159.1:p.Arg633Ter
XM_017024671.2:c.1537C>T XP_016880160.1:p.Arg513Ter
XM_017024672.1:c.1537C>T XP_016880161.1:p.Arg513Ter
XM_017024673.2:c.1264C>T XP_016880162.1:p.Arg422Ter
XM_024450765.1:c.1537C>T XP_024306533.1:p.Arg513Ter