Canonical Allele Identifier: CA499890849

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143311468
• MyVariant Identifiers: chr17:g.37884174A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727921A>T , CM000679.2:g.39727921A>T	GRCh38
NC_000017.10:g.37884174A>T , CM000679.1:g.37884174A>T	GRCh37
NC_000017.9:g.35137700A>T	NCBI36
NG_007503.1:g.44782A>T , LRG_724:g.44782A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3645A>T MANE Select	ENSP00000269571.4:p.Pro1215=
ENST00000269571.9:c.3645A>T	ENSP00000269571.4:p.Pro1215=
ENST00000406381.6:c.3555A>T	ENSP00000385185.2:p.Pro1185=
ENST00000445658.6:c.2817A>T	ENSP00000404047.2:p.Pro939=
ENST00000541774.5:c.3600A>T	ENSP00000446466.1:p.Pro1200=
ENST00000578373.5:c.*3435A>T	ENSP00000463427.1:n.*3435A>T
ENST00000584450.5:c.*224A>T	ENSP00000463714.1:n.*224A>T
ENST00000584601.5:c.3555A>T	ENSP00000462438.1:p.Pro1185=
NM_001005862.2:c.3555A>T , LRG_724t1:c.3555A>T	NP_001005862.1:p.Pro1185=
NM_001289936.1:c.3600A>T , LRG_724t4:c.3600A>T	NP_001276865.1:p.Pro1200=
NM_001289937.1:c.*224A>T	NP_001276866.1:n.*224A>T
NM_004448.3:c.3645A>T , LRG_724t2:c.3645A>T	NP_004439.2:p.Pro1215=
NR_110535.1:n.3969A>T
XM_024450641.1:c.3783A>T	XP_024306409.1:p.Pro1261=
XM_024450642.1:c.3738A>T	XP_024306410.1:p.Pro1246=
XM_024450643.1:c.3693A>T	XP_024306411.1:p.Pro1231=
NM_001005862.3:c.3555A>T	NP_001005862.1:p.Pro1185=
NM_001289936.2:c.3600A>T	NP_001276865.1:p.Pro1200=
NM_001289937.2:c.*224A>T	NP_001276866.1:n.*224A>T
NM_001382782.1:c.3555A>T	NP_001369711.1:p.Pro1185=
NM_001382783.1:c.3555A>T	NP_001369712.1:p.Pro1185=
NM_001382784.1:c.3762A>T	NP_001369713.1:p.Pro1254=
NM_001382785.1:c.3747A>T	NP_001369714.1:p.Pro1249=
NM_001382786.1:c.3726A>T	NP_001369715.1:p.Pro1242=
NM_001382787.1:c.3720A>T	NP_001369716.1:p.Pro1240=
NM_001382788.1:c.3675A>T	NP_001369717.1:p.Pro1225=
NM_001382789.1:c.3666A>T	NP_001369718.1:p.Pro1222=
NM_001382790.1:c.3642A>T	NP_001369719.1:p.Pro1214=
NM_001382791.1:c.3636A>T	NP_001369720.1:p.Pro1212=
NM_001382792.1:c.3609A>T	NP_001369721.1:p.Pro1203=
NM_001382793.1:c.3603A>T	NP_001369722.1:p.Pro1201=
NM_001382794.1:c.3603A>T	NP_001369723.1:p.Pro1201=
NM_001382795.1:c.3597A>T	NP_001369724.1:p.Pro1199=
NM_001382796.1:c.3558A>T	NP_001369725.1:p.Pro1186=
NM_001382797.1:c.3546A>T	NP_001369726.1:p.Pro1182=
NM_001382798.1:c.3489A>T	NP_001369727.1:p.Pro1163=
NM_001382799.1:c.3465A>T	NP_001369728.1:p.Pro1155=
NM_001382800.1:c.3459A>T	NP_001369729.1:p.Pro1153=
NM_001382801.1:c.3441A>T	NP_001369730.1:p.Pro1147=
NM_001382802.1:c.3387A>T	NP_001369731.1:p.Pro1129=
NM_001382803.1:c.*224A>T	NP_001369732.1:n.*224A>T
NM_001382804.1:c.2817A>T	NP_001369733.1:p.Pro939=
NM_001382805.1:c.2694A>T	NP_001369734.1:p.Pro898=
NM_001382806.1:c.2607A>T	NP_001369735.1:p.Pro869=
NM_004448.4:c.3645A>T MANE Select	NP_004439.2:p.Pro1215=
NR_110535.2:n.3883A>T