Canonical Allele Identifier: CA2691415173

Gene: ASTN2 TRIM32

Linked Data

• gnomAD v4: 9-116697781-C-CTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.116697781_116697782insTGG , CM000671.2:g.116697781_116697782insTGG	GRCh38
NC_000009.11:g.119460060_119460061insTGG , CM000671.1:g.119460060_119460061insTGG	GRCh37
NC_000009.10:g.118499881_118499882insTGG	NCBI36
NG_011619.1:g.15480_15481insTGG , LRG_211:g.15480_15481insTGG
NG_021409.1:g.722257_722258insCCA
NG_021409.2:g.722276_722277insCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313400.9:c.2806+27989_2806+27990insCCA (ASTN2) MANE Select	ENSP00000314038.4:n.2806+27989_2806+27990insCCA
ENST00000361477.8:c.2653+27989_2653+27990insCCA (ASTN2)	ENSP00000355116.5:n.2653+27989_2653+27990insCCA
ENST00000450136.2:c.39_40insTGG (TRIM32) MANE Select	ENSP00000408292.1:p.Ala13_Leu14insTrp
ENST00000313400.8:c.2806+27989_2806+27990insCCA (ASTN2)	ENSP00000314038.4:n.2806+27989_2806+27990insCCA
ENST00000361209.6:c.2653+27989_2653+27990insCCA (ASTN2)	ENSP00000354504.2:n.2653+27989_2653+27990insCCA
ENST00000361477.7:c.-39+27989_-39+27990insCCA (ASTN2)	ENSP00000355116.4:n.-39+27989_-39+27990insCCA
ENST00000373983.2:c.39_40insTGG (TRIM32)	ENSP00000363095.1:p.Ala13_Leu14insTrp
ENST00000373986.7:c.1975+27989_1975+27990insCCA (ASTN2)	ENSP00000363098.3:n.1975+27989_1975+27990insCCA
ENST00000411410.1:c.39_40insTGG (TRIM32)	ENSP00000412603.1:p.Ala13_Leu14insTrp
ENST00000450136.1:c.39_40insTGG (TRIM32)	ENSP00000408292.1:p.Ala13_Leu14insTrp
NM_001099679.1:c.39_40insTGG (TRIM32)	NP_001093149.1:p.Ala13_Leu14insTrp
NM_012210.3:c.39_40insTGG , LRG_211t1:c.39_40insTGG (TRIM32)	NP_036342.2:p.Ala13_Leu14insTrp
NM_014010.4:c.2653+27989_2653+27990insCCA (ASTN2)	NP_054729.3:n.2653+27989_2653+27990insCCA
XM_005251813.2:c.39_40insTGG (TRIM32)	XP_005251870.1:p.Ala13_Leu14insTrp
XM_011518396.1:c.39_40insTGG (TRIM32)	XP_011516698.1:p.Ala13_Leu14insTrp
XM_011518397.1:c.39_40insTGG (TRIM32)	XP_011516699.1:p.Ala13_Leu14insTrp
XM_011518398.1:c.39_40insTGG (TRIM32)	XP_011516700.1:p.Ala13_Leu14insTrp
NM_001365068.1:c.2806+27989_2806+27990insCCA (ASTN2) MANE Select	NP_001351997.1:n.2806+27989_2806+27990insCCA
NM_001365069.1:c.2794+27989_2794+27990insCCA (ASTN2)	NP_001351998.1:n.2794+27989_2794+27990insCCA
XM_005251813.4:c.39_40insTGG (TRIM32)	XP_005251870.1:p.Ala13_Leu14insTrp
XM_011518398.2:c.39_40insTGG (TRIM32)	XP_011516700.1:p.Ala13_Leu14insTrp
XM_017014486.1:c.39_40insTGG (TRIM32)	XP_016869975.1:p.Ala13_Leu14insTrp
NM_001099679.2:c.39_40insTGG (TRIM32)	NP_001093149.1:p.Ala13_Leu14insTrp
NM_014010.5:c.2653+27989_2653+27990insCCA (ASTN2)	NP_054729.3:n.2653+27989_2653+27990insCCA
NM_001379048.1:c.39_40insTGG (TRIM32)	NP_001365977.1:p.Ala13_Leu14insTrp
NM_001379049.1:c.39_40insTGG (TRIM32)	NP_001365978.1:p.Ala13_Leu14insTrp
NM_001379050.1:c.39_40insTGG (TRIM32)	NP_001365979.1:p.Ala13_Leu14insTrp
NM_012210.4:c.39_40insTGG (TRIM32) MANE Select	NP_036342.2:p.Ala13_Leu14insTrp