Canonical Allele Identifier: CA2259228698

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727346C= , CM000679.2:g.39727346C=	GRCh38
NC_000017.10:g.37883599C= , CM000679.1:g.37883599C=	GRCh37
NC_000017.9:g.35137125C=	NCBI36
NG_007503.1:g.44207C= , LRG_724:g.44207C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3211C= MANE Select	ENSP00000269571.4:p.Pro1071=
ENST00000269571.9:c.3211C=	ENSP00000269571.4:p.Pro1071=
ENST00000406381.6:c.3121C=	ENSP00000385185.2:p.Pro1041=
ENST00000445658.6:c.2383C=	ENSP00000404047.2:p.Pro795=
ENST00000541774.5:c.3166C=	ENSP00000446466.1:p.Pro1056=
ENST00000578373.5:c.*3001C=	ENSP00000463427.1:n.*3001C=
ENST00000584450.5:c.3160-343C=	ENSP00000463714.1:n.3160-343C=
ENST00000584601.5:c.3121C=	ENSP00000462438.1:p.Pro1041=
NM_001005862.2:c.3121C= , LRG_724t1:c.3121C=	NP_001005862.1:p.Pro1041=
NM_001289936.1:c.3166C= , LRG_724t4:c.3166C=	NP_001276865.1:p.Pro1056=
NM_001289937.1:c.3160-343C=	NP_001276866.1:n.3160-343C=
NM_004448.3:c.3211C= , LRG_724t2:c.3211C=	NP_004439.2:p.Pro1071=
NR_110535.1:n.3535C=
XM_024450641.1:c.3349C=	XP_024306409.1:p.Pro1117=
XM_024450642.1:c.3304C=	XP_024306410.1:p.Pro1102=
XM_024450643.1:c.3259C=	XP_024306411.1:p.Pro1087=
NM_001005862.3:c.3121C=	NP_001005862.1:p.Pro1041=
NM_001289936.2:c.3166C=	NP_001276865.1:p.Pro1056=
NM_001289937.2:c.3160-343C=	NP_001276866.1:n.3160-343C=
NM_001382782.1:c.3121C=	NP_001369711.1:p.Pro1041=
NM_001382783.1:c.3121C=	NP_001369712.1:p.Pro1041=
NM_001382784.1:c.3328C=	NP_001369713.1:p.Pro1110=
NM_001382785.1:c.3313C=	NP_001369714.1:p.Pro1105=
NM_001382786.1:c.3292C=	NP_001369715.1:p.Pro1098=
NM_001382787.1:c.3286C=	NP_001369716.1:p.Pro1096=
NM_001382788.1:c.3241C=	NP_001369717.1:p.Pro1081=
NM_001382789.1:c.3232C=	NP_001369718.1:p.Pro1078=
NM_001382790.1:c.3208C=	NP_001369719.1:p.Pro1070=
NM_001382791.1:c.3202C=	NP_001369720.1:p.Pro1068=
NM_001382792.1:c.3175C=	NP_001369721.1:p.Pro1059=
NM_001382793.1:c.3169C=	NP_001369722.1:p.Pro1057=
NM_001382794.1:c.3169C=	NP_001369723.1:p.Pro1057=
NM_001382795.1:c.3163C=	NP_001369724.1:p.Pro1055=
NM_001382796.1:c.3124C=	NP_001369725.1:p.Pro1042=
NM_001382797.1:c.3112C=	NP_001369726.1:p.Pro1038=
NM_001382798.1:c.3055C=	NP_001369727.1:p.Pro1019=
NM_001382799.1:c.3031C=	NP_001369728.1:p.Pro1011=
NM_001382800.1:c.3025C=	NP_001369729.1:p.Pro1009=
NM_001382801.1:c.3007C=	NP_001369730.1:p.Pro1003=
NM_001382802.1:c.2953C=	NP_001369731.1:p.Pro985=
NM_001382803.1:c.3118-343C=	NP_001369732.1:n.3118-343C=
NM_001382804.1:c.2383C=	NP_001369733.1:p.Pro795=
NM_001382805.1:c.2260C=	NP_001369734.1:p.Pro754=
NM_001382806.1:c.2173C=	NP_001369735.1:p.Pro725=
NM_004448.4:c.3211C= MANE Select	NP_004439.2:p.Pro1071=
NR_110535.2:n.3449C=