Canonical Allele Identifier: CA2788249623

Gene: EGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62814137_62814138insTATTTTTTCA , CM000672.2:g.62814137_62814138insTATTTTTTCA	GRCh38
NC_000010.10:g.64573897_64573898insTATTTTTTCA , CM000672.1:g.64573897_64573898insTATTTTTTCA	GRCh37
NC_000010.9:g.64243903_64243904insTATTTTTTCA	NCBI36
NG_008936.2:g.110763_110764insTGAAAAAATA , LRG_239:g.110763_110764insTGAAAAAATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411732.4:c.350_351insTGAAAAAATA	ENSP00000387634.1:p.Pro118GlufsTer?
ENST00000439032.6:c.1040_1041insTGAAAAAATA	ENSP00000509775.1:n.1040_1041insTGAAAAAATA
ENST00000637191.2:c.500_501insTGAAAAAATA	ENSP00000490154.2:p.Pro168GlufsTer?
ENST00000690143.1:c.*432_*433insTGAAAAAATA	ENSP00000510306.1:n.*432_*433insTGAAAAAATA
ENST00000691610.1:c.539_540insTGAAAAAATA	ENSP00000509830.1:p.Pro181GlufsTer?
ENST00000242480.4:c.500_501insTGAAAAAATA MANE Select	ENSP00000242480.3:p.Pro168GlufsTer?
ENST00000411732.3:c.350_351insTGAAAAAATA	ENSP00000387634.1:p.Pro118GlufsTer?
ENST00000639815.1:n.109-1176_109-1175insTGAAAAAATA
ENST00000242480.3:c.500_501insTGAAAAAATA	ENSP00000242480.3:p.Pro168GlufsTer?
ENST00000411732.2:c.350_351insTGAAAAAATA	ENSP00000387634.1:p.Pro118GlufsTer?
ENST00000439032.4:c.500_501insTGAAAAAATA	ENSP00000402040.1:p.Pro168GlufsTer?
NM_000399.3:c.500_501insTGAAAAAATA , LRG_239t1:c.500_501insTGAAAAAATA	NP_000390.2:p.Pro168GlufsTer?
NM_001136177.1:c.500_501insTGAAAAAATA	NP_001129649.1:p.Pro168GlufsTer?
NM_001136178.1:c.500_501insTGAAAAAATA	NP_001129650.1:p.Pro168GlufsTer?
NM_001136179.1:c.350_351insTGAAAAAATA	NP_001129651.1:p.Pro118GlufsTer?
XM_011539427.1:c.539_540insTGAAAAAATA	XP_011537729.1:p.Pro181GlufsTer?
XM_011539428.1:c.350_351insTGAAAAAATA	XP_011537730.1:p.Pro118GlufsTer?
XM_011539429.1:c.350_351insTGAAAAAATA	XP_011537731.1:p.Pro118GlufsTer?
NM_000399.4:c.500_501insTGAAAAAATA	NP_000390.2:p.Pro168GlufsTer?
NM_001136177.2:c.500_501insTGAAAAAATA	NP_001129649.1:p.Pro168GlufsTer?
NM_001136179.2:c.350_351insTGAAAAAATA	NP_001129651.1:p.Pro118GlufsTer?
NM_001321037.1:c.350_351insTGAAAAAATA	NP_001307966.1:p.Pro118GlufsTer?
NM_000399.5:c.500_501insTGAAAAAATA MANE Select	NP_000390.2:p.Pro168GlufsTer?
NM_001136177.3:c.500_501insTGAAAAAATA	NP_001129649.1:p.Pro168GlufsTer?
NM_001136179.3:c.350_351insTGAAAAAATA	NP_001129651.1:p.Pro118GlufsTer?
NM_001321037.2:c.350_351insTGAAAAAATA	NP_001307966.1:p.Pro118GlufsTer?
NM_001136178.2:c.500_501insTGAAAAAATA	NP_001129650.1:p.Pro168GlufsTer?