Canonical Allele Identifier: CA2259229153

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727545C= , CM000679.2:g.39727545C=	GRCh38
NC_000017.10:g.37883798C= , CM000679.1:g.37883798C=	GRCh37
NC_000017.9:g.35137324C=	NCBI36
NG_007503.1:g.44406C= , LRG_724:g.44406C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3410C= MANE Select	ENSP00000269571.4:p.Pro1137=
ENST00000269571.9:c.3410C=	ENSP00000269571.4:p.Pro1137=
ENST00000406381.6:c.3320C=	ENSP00000385185.2:p.Pro1107=
ENST00000445658.6:c.2582C=	ENSP00000404047.2:p.Pro861=
ENST00000541774.5:c.3365C=	ENSP00000446466.1:p.Pro1122=
ENST00000578373.5:c.*3200C=	ENSP00000463427.1:n.*3200C=
ENST00000584450.5:c.3160-144C=	ENSP00000463714.1:n.3160-144C=
ENST00000584601.5:c.3320C=	ENSP00000462438.1:p.Pro1107=
NM_001005862.2:c.3320C= , LRG_724t1:c.3320C=	NP_001005862.1:p.Pro1107=
NM_001289936.1:c.3365C= , LRG_724t4:c.3365C=	NP_001276865.1:p.Pro1122=
NM_001289937.1:c.3160-144C=	NP_001276866.1:n.3160-144C=
NM_004448.3:c.3410C= , LRG_724t2:c.3410C=	NP_004439.2:p.Pro1137=
NR_110535.1:n.3734C=
XM_024450641.1:c.3548C=	XP_024306409.1:p.Pro1183=
XM_024450642.1:c.3503C=	XP_024306410.1:p.Pro1168=
XM_024450643.1:c.3458C=	XP_024306411.1:p.Pro1153=
NM_001005862.3:c.3320C=	NP_001005862.1:p.Pro1107=
NM_001289936.2:c.3365C=	NP_001276865.1:p.Pro1122=
NM_001289937.2:c.3160-144C=	NP_001276866.1:n.3160-144C=
NM_001382782.1:c.3320C=	NP_001369711.1:p.Pro1107=
NM_001382783.1:c.3320C=	NP_001369712.1:p.Pro1107=
NM_001382784.1:c.3527C=	NP_001369713.1:p.Pro1176=
NM_001382785.1:c.3512C=	NP_001369714.1:p.Pro1171=
NM_001382786.1:c.3491C=	NP_001369715.1:p.Pro1164=
NM_001382787.1:c.3485C=	NP_001369716.1:p.Pro1162=
NM_001382788.1:c.3440C=	NP_001369717.1:p.Pro1147=
NM_001382789.1:c.3431C=	NP_001369718.1:p.Pro1144=
NM_001382790.1:c.3407C=	NP_001369719.1:p.Pro1136=
NM_001382791.1:c.3401C=	NP_001369720.1:p.Pro1134=
NM_001382792.1:c.3374C=	NP_001369721.1:p.Pro1125=
NM_001382793.1:c.3368C=	NP_001369722.1:p.Pro1123=
NM_001382794.1:c.3368C=	NP_001369723.1:p.Pro1123=
NM_001382795.1:c.3362C=	NP_001369724.1:p.Pro1121=
NM_001382796.1:c.3323C=	NP_001369725.1:p.Pro1108=
NM_001382797.1:c.3311C=	NP_001369726.1:p.Pro1104=
NM_001382798.1:c.3254C=	NP_001369727.1:p.Pro1085=
NM_001382799.1:c.3230C=	NP_001369728.1:p.Pro1077=
NM_001382800.1:c.3224C=	NP_001369729.1:p.Pro1075=
NM_001382801.1:c.3206C=	NP_001369730.1:p.Pro1069=
NM_001382802.1:c.3152C=	NP_001369731.1:p.Pro1051=
NM_001382803.1:c.3118-144C=	NP_001369732.1:n.3118-144C=
NM_001382804.1:c.2582C=	NP_001369733.1:p.Pro861=
NM_001382805.1:c.2459C=	NP_001369734.1:p.Pro820=
NM_001382806.1:c.2372C=	NP_001369735.1:p.Pro791=
NM_004448.4:c.3410C= MANE Select	NP_004439.2:p.Pro1137=
NR_110535.2:n.3648C=