Canonical Allele Identifier: CA2637622660

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39711919-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39711922_39711924del , CM000679.2:g.39711922_39711924del	GRCh38
NC_000017.10:g.37868175_37868177del , CM000679.1:g.37868175_37868177del	GRCh37
NC_000017.9:g.35121701_35121703del	NCBI36
NG_007503.1:g.28783_28785del , LRG_724:g.28783_28785del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.902-6_902-4del MANE Select	ENSP00000269571.4:n.902-6_902-4del
ENST00000269571.9:c.902-6_902-4del	ENSP00000269571.4:n.902-6_902-4del
ENST00000406381.6:c.812-6_812-4del	ENSP00000385185.2:n.812-6_812-4del
ENST00000445658.6:c.74-6_74-4del	ENSP00000404047.2:n.74-6_74-4del
ENST00000541774.5:c.857-6_857-4del	ENSP00000446466.1:n.857-6_857-4del
ENST00000578199.5:c.812-6_812-4del	ENSP00000462808.1:n.812-6_812-4del
ENST00000578373.5:c.*692-6_*692-4del	ENSP00000463427.1:n.*692-6_*692-4del
ENST00000578502.1:c.127-6_127-4del
ENST00000582648.5:c.226-6_226-4del	ENSP00000462024.1:n.226-6_226-4del
ENST00000582788.5:n.391-6_391-4del
ENST00000583038.5:n.1594-6_1594-4del
ENST00000584450.5:c.902-6_902-4del	ENSP00000463714.1:n.902-6_902-4del
ENST00000584601.5:c.812-6_812-4del	ENSP00000462438.1:n.812-6_812-4del
ENST00000584908.5:n.914-6_914-4del
NM_001005862.2:c.812-6_812-4del , LRG_724t1:c.812-6_812-4del	NP_001005862.1:n.812-6_812-4del
NM_001289936.1:c.857-6_857-4del , LRG_724t4:c.857-6_857-4del	NP_001276865.1:n.857-6_857-4del
NM_001289937.1:c.902-6_902-4del	NP_001276866.1:n.902-6_902-4del
NM_001289938.1:c.812-6_812-4del , LRG_724t3:c.812-6_812-4del	NP_001276867.1:n.812-6_812-4del
NM_004448.3:c.902-6_902-4del , LRG_724t2:c.902-6_902-4del	NP_004439.2:n.902-6_902-4del
NR_110535.1:n.1226-6_1226-4del
XM_024450641.1:c.1040-6_1040-4del	XP_024306409.1:n.1040-6_1040-4del
XM_024450642.1:c.995-6_995-4del	XP_024306410.1:n.995-6_995-4del
XM_024450643.1:c.950-6_950-4del	XP_024306411.1:n.950-6_950-4del
NM_001005862.3:c.812-6_812-4del	NP_001005862.1:n.812-6_812-4del
NM_001289936.2:c.857-6_857-4del	NP_001276865.1:n.857-6_857-4del
NM_001289937.2:c.902-6_902-4del	NP_001276866.1:n.902-6_902-4del
NM_001289938.2:c.812-6_812-4del	NP_001276867.1:n.812-6_812-4del
NM_001382782.1:c.812-6_812-4del	NP_001369711.1:n.812-6_812-4del
NM_001382783.1:c.812-6_812-4del	NP_001369712.1:n.812-6_812-4del
NM_001382784.1:c.902-6_902-4del	NP_001369713.1:n.902-6_902-4del
NM_001382785.1:c.902-6_902-4del	NP_001369714.1:n.902-6_902-4del
NM_001382786.1:c.902-6_902-4del	NP_001369715.1:n.902-6_902-4del
NM_001382787.1:c.977-6_977-4del	NP_001369716.1:n.977-6_977-4del
NM_001382788.1:c.902-6_902-4del	NP_001369717.1:n.902-6_902-4del
NM_001382789.1:c.902-6_902-4del	NP_001369718.1:n.902-6_902-4del
NM_001382790.1:c.902-6_902-4del	NP_001369719.1:n.902-6_902-4del
NM_001382791.1:c.893-6_893-4del	NP_001369720.1:n.893-6_893-4del
NM_001382792.1:c.902-6_902-4del	NP_001369721.1:n.902-6_902-4del
NM_001382793.1:c.902-6_902-4del	NP_001369722.1:n.902-6_902-4del
NM_001382794.1:c.902-6_902-4del	NP_001369723.1:n.902-6_902-4del
NM_001382795.1:c.902-6_902-4del	NP_001369724.1:n.902-6_902-4del
NM_001382796.1:c.902-6_902-4del	NP_001369725.1:n.902-6_902-4del
NM_001382797.1:c.902-6_902-4del	NP_001369726.1:n.902-6_902-4del
NM_001382798.1:c.902-6_902-4del	NP_001369727.1:n.902-6_902-4del
NM_001382799.1:c.722-6_722-4del	NP_001369728.1:n.722-6_722-4del
NM_001382800.1:c.902-6_902-4del	NP_001369729.1:n.902-6_902-4del
NM_001382801.1:c.902-6_902-4del	NP_001369730.1:n.902-6_902-4del
NM_001382802.1:c.644-6_644-4del	NP_001369731.1:n.644-6_644-4del
NM_001382803.1:c.902-6_902-4del	NP_001369732.1:n.902-6_902-4del
NM_001382804.1:c.74-6_74-4del	NP_001369733.1:n.74-6_74-4del
NM_001382805.1:c.902-6_902-4del	NP_001369734.1:n.902-6_902-4del
NM_001382806.1:c.902-6_902-4del	NP_001369735.1:n.902-6_902-4del
NM_004448.4:c.902-6_902-4del MANE Select	NP_004439.2:n.902-6_902-4del
NR_110535.2:n.1140-6_1140-4del