Canonical Allele Identifier: CA2691415180

Gene: ASTN2 TRIM32

Linked Data

• gnomAD v4: 9-116698260-T-TACTTGACTTTCTTAATCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.116698260_116698261insACTTGACTTTCTTAATCC , CM000671.2:g.116698260_116698261insACTTGACTTTCTTAATCC	GRCh38
NC_000009.11:g.119460539_119460540insACTTGACTTTCTTAATCC , CM000671.1:g.119460539_119460540insACTTGACTTTCTTAATCC	GRCh37
NC_000009.10:g.118500360_118500361insACTTGACTTTCTTAATCC	NCBI36
NG_011619.1:g.15959_15960insACTTGACTTTCTTAATCC , LRG_211:g.15959_15960insACTTGACTTTCTTAATCC
NG_021409.1:g.721778_721779insGGATTAAGAAAGTCAAGT
NG_021409.2:g.721797_721798insGGATTAAGAAAGTCAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313400.9:c.2806+27510_2806+27511insGGATTAAGAAAGTCAAGT (ASTN2) MANE Select	ENSP00000314038.4:n.2806+27510_2806+27511insGGATTAAGAAAGTCAAG...
ENST00000361477.8:c.2653+27510_2653+27511insGGATTAAGAAAGTCAAGT (ASTN2)	ENSP00000355116.5:n.2653+27510_2653+27511insGGATTAAGAAAGTCAAG...
ENST00000450136.2:c.518_519insACTTGACTTTCTTAATCC (TRIM32) MANE Select	ENSP00000408292.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
ENST00000313400.8:c.2806+27510_2806+27511insGGATTAAGAAAGTCAAGT (ASTN2)	ENSP00000314038.4:n.2806+27510_2806+27511insGGATTAAGAAAGTCAAG...
ENST00000361209.6:c.2653+27510_2653+27511insGGATTAAGAAAGTCAAGT (ASTN2)	ENSP00000354504.2:n.2653+27510_2653+27511insGGATTAAGAAAGTCAAG...
ENST00000361477.7:c.-39+27510_-39+27511insGGATTAAGAAAGTCAAGT (ASTN2)	ENSP00000355116.4:n.-39+27510_-39+27511insGGATTAAGAAAGTCAAGT
ENST00000373983.2:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	ENSP00000363095.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
ENST00000373986.7:c.1975+27510_1975+27511insGGATTAAGAAAGTCAAGT (ASTN2)	ENSP00000363098.3:n.1975+27510_1975+27511insGGATTAAGAAAGTCAAG...
ENST00000450136.1:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	ENSP00000408292.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
NM_001099679.1:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	NP_001093149.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
NM_012210.3:c.518_519insACTTGACTTTCTTAATCC , LRG_211t1:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	NP_036342.2:p.Val173_Ser174insLeuAspPheLeuAsnPro
NM_014010.4:c.2653+27510_2653+27511insGGATTAAGAAAGTCAAGT (ASTN2)	NP_054729.3:n.2653+27510_2653+27511insGGATTAAGAAAGTCAAGT
XM_005251813.2:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	XP_005251870.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
XM_011518396.1:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	XP_011516698.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
XM_011518397.1:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	XP_011516699.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
XM_011518398.1:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	XP_011516700.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
NM_001365068.1:c.2806+27510_2806+27511insGGATTAAGAAAGTCAAGT (ASTN2) MANE Select	NP_001351997.1:n.2806+27510_2806+27511insGGATTAAGAAAGTCAAGT
NM_001365069.1:c.2794+27510_2794+27511insGGATTAAGAAAGTCAAGT (ASTN2)	NP_001351998.1:n.2794+27510_2794+27511insGGATTAAGAAAGTCAAGT
XM_005251813.4:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	XP_005251870.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
XM_011518398.2:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	XP_011516700.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
XM_017014486.1:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	XP_016869975.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
NM_001099679.2:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	NP_001093149.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
NM_014010.5:c.2653+27510_2653+27511insGGATTAAGAAAGTCAAGT (ASTN2)	NP_054729.3:n.2653+27510_2653+27511insGGATTAAGAAAGTCAAGT
NM_001379048.1:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	NP_001365977.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
NM_001379049.1:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	NP_001365978.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
NM_001379050.1:c.518_519insACTTGACTTTCTTAATCC (TRIM32)	NP_001365979.1:p.Val173_Ser174insLeuAspPheLeuAsnPro
NM_012210.4:c.518_519insACTTGACTTTCTTAATCC (TRIM32) MANE Select	NP_036342.2:p.Val173_Ser174insLeuAspPheLeuAsnPro