Canonical Allele Identifier: CA2682856341

Gene: EGFR

Linked Data

• gnomAD v4: 7-55201247-G-GCTCCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55201247_55201248insCTCCTC , CM000669.2:g.55201247_55201248insCTCCTC	GRCh38
NC_000007.13:g.55268940_55268941insCTCCTC , CM000669.1:g.55268940_55268941insCTCCTC	GRCh37
NC_000007.12:g.55236434_55236435insCTCCTC	NCBI36
NG_007726.3:g.187216_187217insCTCCTC , LRG_304:g.187216_187217insCTCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2847_2848insCTCCTC	ENSP00000413354.2:p.Met949_Asp950insLeuLeu
ENST00000700145.1:c.900-4100_900-4099insCTCCTC
ENST00000700146.1:n.750_751insCTCCTC
ENST00000700147.1:n.675_676insCTCCTC
ENST00000275493.7:c.3006_3007insCTCCTC MANE Select	ENSP00000275493.2:p.Met1002_Asp1003insLeuLeu
ENST00000275493.6:c.3006_3007insCTCCTC	ENSP00000275493.2:p.Met1002_Asp1003insLeuLeu
ENST00000442591.5:c.*28+28319_*28+28320insCTCCTC	ENSP00000410031.1:n.*28+28319_*28+28320insCTCCTC
ENST00000454757.6:c.2871_2872insCTCCTC	ENSP00000395243.3:p.Met957_Asp958insLeuLeu
ENST00000455089.5:c.2871_2872insCTCCTC	ENSP00000415559.1:p.Met957_Asp958insLeuLeu
NM_005228.3:c.3006_3007insCTCCTC , LRG_304t1:c.3006_3007insCTCCTC	NP_005219.2:p.Met1002_Asp1003insLeuLeu
NM_001346897.1:c.2871_2872insCTCCTC	NP_001333826.1:p.Met957_Asp958insLeuLeu
NM_001346898.1:c.3006_3007insCTCCTC	NP_001333827.1:p.Met1002_Asp1003insLeuLeu
NM_001346899.1:c.2871_2872insCTCCTC	NP_001333828.1:p.Met957_Asp958insLeuLeu
NM_001346900.1:c.2847_2848insCTCCTC	NP_001333829.1:p.Met949_Asp950insLeuLeu
NM_001346941.1:c.2205_2206insCTCCTC	NP_001333870.1:p.Met735_Asp736insLeuLeu
NM_005228.4:c.3006_3007insCTCCTC	NP_005219.2:p.Met1002_Asp1003insLeuLeu
NM_005228.5:c.3006_3007insCTCCTC MANE Select	NP_005219.2:p.Met1002_Asp1003insLeuLeu
NM_001346897.2:c.2871_2872insCTCCTC	NP_001333826.1:p.Met957_Asp958insLeuLeu
NM_001346898.2:c.3006_3007insCTCCTC	NP_001333827.1:p.Met1002_Asp1003insLeuLeu
NM_001346900.2:c.2847_2848insCTCCTC	NP_001333829.1:p.Met949_Asp950insLeuLeu
NM_001346941.2:c.2205_2206insCTCCTC	NP_001333870.1:p.Met735_Asp736insLeuLeu
NM_001346899.2:c.2871_2872insCTCCTC	NP_001333828.1:p.Met957_Asp958insLeuLeu