Canonical Allele Identifier: CA645561559

Gene: EGFR EGFR-AS1

Linked Data

• dbSNP Id: rs2128958264
• COSMIC: COSM12425

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181311_55181312insCGCTGGCCA , CM000669.2:g.55181311_55181312insCGCTGGCCA	GRCh38
NC_000007.13:g.55249004_55249005insCGCTGGCCA , CM000669.1:g.55249004_55249005insCGCTGGCCA	GRCh37
NC_000007.12:g.55216498_55216499insCGCTGGCCA	NCBI36
NG_007726.3:g.167280_167281insCGCTGGCCA , LRG_304:g.167280_167281insCGCTGGCCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2143_2144insCGCTGGCCA (EGFR)	ENSP00000413354.2:p.Ala714_Ser715insThrLe...
ENST00000700145.1:c.651_652insCGCTGGCCA (EGFR)
ENST00000275493.7:c.2302_2303insCGCTGGCCA (EGFR) MANE Select	ENSP00000275493.2:p.Ala767_Ser768insThrLe...
ENST00000275493.6:c.2302_2303insCGCTGGCCA (EGFR)	ENSP00000275493.2:p.Ala767_Ser768insThrLe...
ENST00000442591.5:c.*28+8383_*28+8384insCGCTGGCCA (EGFR)	ENSP00000410031.1:n.*28+8383_*28+8384insC...
ENST00000454757.6:c.2167_2168insCGCTGGCCA (EGFR)	ENSP00000395243.3:p.Ala722_Ser723insThrLe...
ENST00000455089.5:c.2167_2168insCGCTGGCCA (EGFR)	ENSP00000415559.1:p.Ala722_Ser723insThrLe...
NM_005228.3:c.2302_2303insCGCTGGCCA , LRG_304t1:c.2302_2303insCGCTGGCCA (EGFR)	NP_005219.2:p.Ala767_Ser768insThrLeuAla
NR_047551.1:n.1265_1266insGCGTGGCCA (EGFR-AS1)
NM_001346897.1:c.2167_2168insCGCTGGCCA (EGFR)	NP_001333826.1:p.Ala722_Ser723insThrLeuAl...
NM_001346898.1:c.2302_2303insCGCTGGCCA (EGFR)	NP_001333827.1:p.Ala767_Ser768insThrLeuAl...
NM_001346899.1:c.2167_2168insCGCTGGCCA (EGFR)	NP_001333828.1:p.Ala722_Ser723insThrLeuAl...
NM_001346900.1:c.2143_2144insCGCTGGCCA (EGFR)	NP_001333829.1:p.Ala714_Ser715insThrLeuAl...
NM_001346941.1:c.1501_1502insCGCTGGCCA (EGFR)	NP_001333870.1:p.Ala500_Ser501insThrLeuAl...
NM_005228.4:c.2302_2303insCGCTGGCCA (EGFR)	NP_005219.2:p.Ala767_Ser768insThrLeuAla
NM_005228.5:c.2302_2303insCGCTGGCCA (EGFR) MANE Select	NP_005219.2:p.Ala767_Ser768insThrLeuAla
NM_001346897.2:c.2167_2168insCGCTGGCCA (EGFR)	NP_001333826.1:p.Ala722_Ser723insThrLeuAl...
NM_001346898.2:c.2302_2303insCGCTGGCCA (EGFR)	NP_001333827.1:p.Ala767_Ser768insThrLeuAl...
NM_001346900.2:c.2143_2144insCGCTGGCCA (EGFR)	NP_001333829.1:p.Ala714_Ser715insThrLeuAl...
NM_001346941.2:c.1501_1502insCGCTGGCCA (EGFR)	NP_001333870.1:p.Ala500_Ser501insThrLeuAl...
NM_001346899.2:c.2167_2168insCGCTGGCCA (EGFR)	NP_001333828.1:p.Ala722_Ser723insThrLeuAl...