Canonical Allele Identifier: CA2639026730

Gene: TRIM37

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.59083943_59083946del , CM000679.2:g.59083943_59083946del	GRCh38
NC_000017.10:g.57161304_57161307del , CM000679.1:g.57161304_57161307del	GRCh37
NC_000017.9:g.54516086_54516089del	NCBI36
NG_009298.1:g.27962_27965del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262294.12:c.369+58_369+61del MANE Select	ENSP00000262294.7:n.369+58_369+61del
ENST00000262294.11:c.369+58_369+61del	ENSP00000262294.7:n.369+58_369+61del
ENST00000393065.6:c.267+58_267+61del	ENSP00000376784.2:n.267+58_267+61del
ENST00000393066.7:c.369+58_369+61del	ENSP00000376785.3:n.369+58_369+61del
ENST00000577554.5:c.*241+58_*241+61del	ENSP00000462340.1:n.*241+58_*241+61del
ENST00000580122.5:c.280-2725_280-2722del
ENST00000580973.5:c.165-4067_165-4064del	ENSP00000464590.1:n.165-4067_165-4064del
NM_001005207.2:c.369+58_369+61del	NP_001005207.1:n.369+58_369+61del
NM_015294.3:c.369+58_369+61del	NP_056109.1:n.369+58_369+61del
XM_005257385.1:c.369+58_369+61del	XP_005257442.1:n.369+58_369+61del
XM_005257387.1:c.267+58_267+61del	XP_005257444.1:n.267+58_267+61del
XM_005257389.1:c.369+58_369+61del	XP_005257446.1:n.369+58_369+61del
XM_005257390.1:c.369+58_369+61del	XP_005257447.1:n.369+58_369+61del
XM_011524831.1:c.369+58_369+61del	XP_011523133.1:n.369+58_369+61del
XM_011524832.1:c.369+58_369+61del	XP_011523134.1:n.369+58_369+61del
XM_011524833.1:c.369+58_369+61del	XP_011523135.1:n.369+58_369+61del
XM_011524834.1:c.267+58_267+61del	XP_011523136.1:n.267+58_267+61del
XM_011524835.1:c.369+58_369+61del	XP_011523137.1:n.369+58_369+61del
XM_011524836.1:c.369+58_369+61del	XP_011523138.1:n.369+58_369+61del
XM_011524837.1:c.369+58_369+61del	XP_011523139.1:n.369+58_369+61del
NM_001005207.4:c.369+58_369+61del	NP_001005207.1:n.369+58_369+61del
NM_001320987.2:c.267+58_267+61del	NP_001307916.1:n.267+58_267+61del
NM_001320988.2:c.369+58_369+61del	NP_001307917.1:n.369+58_369+61del
NM_001320989.2:c.369+58_369+61del	NP_001307918.1:n.369+58_369+61del
NM_001320990.2:c.3+58_3+61del	NP_001307919.1:n.3+58_3+61del
NM_001353082.1:c.267+58_267+61del	NP_001340011.1:n.267+58_267+61del
NM_001353083.1:c.-384+58_-384+61del	NP_001340012.1:n.-384+58_-384+61del
NM_001353084.1:c.369+58_369+61del	NP_001340013.1:n.369+58_369+61del
NM_001353085.1:c.-93-2725_-93-2722del	NP_001340014.1:n.-93-2725_-93-2722del
NM_001353086.1:c.369+58_369+61del	NP_001340015.1:n.369+58_369+61del
NM_015294.5:c.369+58_369+61del	NP_056109.1:n.369+58_369+61del
NR_148346.1:n.872+58_872+61del
NR_148347.1:n.770+58_770+61del
XM_011524832.2:c.369+58_369+61del	XP_011523134.1:n.369+58_369+61del
XM_017024662.1:c.369+58_369+61del	XP_016880151.1:n.369+58_369+61del
XM_017024663.2:c.369+58_369+61del	XP_016880152.1:n.369+58_369+61del
XM_017024664.1:c.369+58_369+61del	XP_016880153.1:n.369+58_369+61del
XM_017024665.1:c.267+58_267+61del	XP_016880154.1:n.267+58_267+61del
XM_017024667.1:c.369+58_369+61del	XP_016880156.1:n.369+58_369+61del
XM_017024669.2:c.267+58_267+61del	XP_016880158.1:n.267+58_267+61del
XM_017024670.2:c.267+58_267+61del	XP_016880159.1:n.267+58_267+61del
XM_017024671.2:c.-93-2725_-93-2722del	XP_016880160.1:n.-93-2725_-93-2722del
XM_017024672.1:c.-93-2725_-93-2722del	XP_016880161.1:n.-93-2725_-93-2722del
XM_017024673.2:c.-384+58_-384+61del	XP_016880162.1:n.-384+58_-384+61del
XM_024450765.1:c.-93-2725_-93-2722del	XP_024306533.1:n.-93-2725_-93-2722del
NM_015294.6:c.369+58_369+61del MANE Select	NP_056109.1:n.369+58_369+61del
NM_001005207.5:c.369+58_369+61del	NP_001005207.1:n.369+58_369+61del
NM_001320987.3:c.267+58_267+61del	NP_001307916.1:n.267+58_267+61del
NM_001320988.3:c.369+58_369+61del	NP_001307917.1:n.369+58_369+61del
NM_001320989.3:c.369+58_369+61del	NP_001307918.1:n.369+58_369+61del
NM_001320990.3:c.3+58_3+61del	NP_001307919.1:n.3+58_3+61del
NM_001353082.2:c.267+58_267+61del	NP_001340011.1:n.267+58_267+61del
NM_001353083.2:c.-384+58_-384+61del	NP_001340012.1:n.-384+58_-384+61del
NM_001353084.2:c.369+58_369+61del	NP_001340013.1:n.369+58_369+61del
NM_001353085.2:c.-93-2725_-93-2722del	NP_001340014.1:n.-93-2725_-93-2722del
NM_001353086.2:c.369+58_369+61del	NP_001340015.1:n.369+58_369+61del
NR_148346.2:n.788+58_788+61del
NR_148347.2:n.686+58_686+61del