Canonical Allele Identifier: CA499671663

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883673C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727420C>T , CM000679.2:g.39727420C>T	GRCh38
NC_000017.10:g.37883673C>T , CM000679.1:g.37883673C>T	GRCh37
NC_000017.9:g.35137199C>T	NCBI36
NG_007503.1:g.44281C>T , LRG_724:g.44281C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3285C>T MANE Select	ENSP00000269571.4:p.Ala1095=
ENST00000269571.9:c.3285C>T	ENSP00000269571.4:p.Ala1095=
ENST00000406381.6:c.3195C>T	ENSP00000385185.2:p.Ala1065=
ENST00000445658.6:c.2457C>T	ENSP00000404047.2:p.Ala819=
ENST00000541774.5:c.3240C>T	ENSP00000446466.1:p.Ala1080=
ENST00000578373.5:c.*3075C>T	ENSP00000463427.1:n.*3075C>T
ENST00000584450.5:c.3160-269C>T	ENSP00000463714.1:n.3160-269C>T
ENST00000584601.5:c.3195C>T	ENSP00000462438.1:p.Ala1065=
NM_001005862.2:c.3195C>T , LRG_724t1:c.3195C>T	NP_001005862.1:p.Ala1065=
NM_001289936.1:c.3240C>T , LRG_724t4:c.3240C>T	NP_001276865.1:p.Ala1080=
NM_001289937.1:c.3160-269C>T	NP_001276866.1:n.3160-269C>T
NM_004448.3:c.3285C>T , LRG_724t2:c.3285C>T	NP_004439.2:p.Ala1095=
NR_110535.1:n.3609C>T
XM_024450641.1:c.3423C>T	XP_024306409.1:p.Ala1141=
XM_024450642.1:c.3378C>T	XP_024306410.1:p.Ala1126=
XM_024450643.1:c.3333C>T	XP_024306411.1:p.Ala1111=
NM_001005862.3:c.3195C>T	NP_001005862.1:p.Ala1065=
NM_001289936.2:c.3240C>T	NP_001276865.1:p.Ala1080=
NM_001289937.2:c.3160-269C>T	NP_001276866.1:n.3160-269C>T
NM_001382782.1:c.3195C>T	NP_001369711.1:p.Ala1065=
NM_001382783.1:c.3195C>T	NP_001369712.1:p.Ala1065=
NM_001382784.1:c.3402C>T	NP_001369713.1:p.Ala1134=
NM_001382785.1:c.3387C>T	NP_001369714.1:p.Ala1129=
NM_001382786.1:c.3366C>T	NP_001369715.1:p.Ala1122=
NM_001382787.1:c.3360C>T	NP_001369716.1:p.Ala1120=
NM_001382788.1:c.3315C>T	NP_001369717.1:p.Ala1105=
NM_001382789.1:c.3306C>T	NP_001369718.1:p.Ala1102=
NM_001382790.1:c.3282C>T	NP_001369719.1:p.Ala1094=
NM_001382791.1:c.3276C>T	NP_001369720.1:p.Ala1092=
NM_001382792.1:c.3249C>T	NP_001369721.1:p.Ala1083=
NM_001382793.1:c.3243C>T	NP_001369722.1:p.Ala1081=
NM_001382794.1:c.3243C>T	NP_001369723.1:p.Ala1081=
NM_001382795.1:c.3237C>T	NP_001369724.1:p.Ala1079=
NM_001382796.1:c.3198C>T	NP_001369725.1:p.Ala1066=
NM_001382797.1:c.3186C>T	NP_001369726.1:p.Ala1062=
NM_001382798.1:c.3129C>T	NP_001369727.1:p.Ala1043=
NM_001382799.1:c.3105C>T	NP_001369728.1:p.Ala1035=
NM_001382800.1:c.3099C>T	NP_001369729.1:p.Ala1033=
NM_001382801.1:c.3081C>T	NP_001369730.1:p.Ala1027=
NM_001382802.1:c.3027C>T	NP_001369731.1:p.Ala1009=
NM_001382803.1:c.3118-269C>T	NP_001369732.1:n.3118-269C>T
NM_001382804.1:c.2457C>T	NP_001369733.1:p.Ala819=
NM_001382805.1:c.2334C>T	NP_001369734.1:p.Ala778=
NM_001382806.1:c.2247C>T	NP_001369735.1:p.Ala749=
NM_004448.4:c.3285C>T MANE Select	NP_004439.2:p.Ala1095=
NR_110535.2:n.3523C>T