Canonical Allele Identifier: CA1671940135

Gene: SUMO4 TAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149400573G= , CM000668.2:g.149400573G=	GRCh38
NC_000006.11:g.149721709G= , CM000668.1:g.149721709G=	GRCh37
NC_000006.10:g.149763402G=	NCBI36
NG_012301.1:g.5215G=
NG_021386.1:g.87274G=
NG_021386.2:g.187650G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326669.6:c.182G= (SUMO4) MANE Select	ENSP00000318635.4:p.Arg61=
ENST00000636456.1:c.1087+1389G= (TAB2)	ENSP00000490379.1:n.1087+1389G=
ENST00000637181.2:c.1939+1389G= (TAB2) MANE Select	ENSP00000490618.1:n.1939+1389G=
ENST00000326669.5:c.182G= (SUMO4)	ENSP00000318635.4:p.Arg61=
ENST00000367456.5:c.1939+1389G= (TAB2)	ENSP00000356426.1:n.1939+1389G=
ENST00000470466.5:c.*538+1389G= (TAB2)	ENSP00000432709.1:n.*538+1389G=
ENST00000484505.1:n.452+1389G= (TAB2)
ENST00000538427.5:c.1939+1389G= (TAB2)	ENSP00000445752.1:n.1939+1389G=
NM_001002255.1:c.182G= (SUMO4)	NP_001002255.1:p.Arg61=
NM_001292034.2:c.1939+1389G= (TAB2)	NP_001278963.1:n.1939+1389G=
NM_001292035.2:c.1843+1389G= (TAB2)	NP_001278964.1:n.1843+1389G=
NM_015093.5:c.1939+1389G= (TAB2)	NP_055908.1:n.1939+1389G=
XM_006715403.2:c.1939+1389G= (TAB2)	XP_006715466.1:n.1939+1389G=
XM_011535633.1:c.1939+1389G= (TAB2)	XP_011533935.1:n.1939+1389G=
XM_011535634.1:c.1939+1389G= (TAB2)	XP_011533936.1:n.1939+1389G=
XM_011535633.2:c.1939+1389G= (TAB2)	XP_011533935.1:n.1939+1389G=
XM_017010591.1:c.1939+1389G= (TAB2)	XP_016866080.1:n.1939+1389G=
XM_017010592.2:c.1939+1389G= (TAB2)	XP_016866081.1:n.1939+1389G=
NM_001292034.3:c.1939+1389G= (TAB2) MANE Select	NP_001278963.1:n.1939+1389G=
NM_001002255.2:c.182G= (SUMO4) MANE Select	NP_001002255.1:p.Arg61=
NM_001292035.3:c.1843+1389G= (TAB2)	NP_001278964.1:n.1843+1389G=
NM_001369506.1:c.1939+1389G= (TAB2)	NP_001356435.1:n.1939+1389G=
NM_015093.6:c.1939+1389G= (TAB2)	NP_055908.1:n.1939+1389G=