Canonical Allele Identifier: CA499890596

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143292961
• MyVariant Identifiers: chr17:g.37884006T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727753T>C , CM000679.2:g.39727753T>C	GRCh38
NC_000017.10:g.37884006T>C , CM000679.1:g.37884006T>C	GRCh37
NC_000017.9:g.35137532T>C	NCBI36
NG_007503.1:g.44614T>C , LRG_724:g.44614T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3477T>C MANE Select	ENSP00000269571.4:p.Ala1159=
ENST00000269571.9:c.3477T>C	ENSP00000269571.4:p.Ala1159=
ENST00000406381.6:c.3387T>C	ENSP00000385185.2:p.Ala1129=
ENST00000445658.6:c.2649T>C	ENSP00000404047.2:p.Ala883=
ENST00000541774.5:c.3432T>C	ENSP00000446466.1:p.Ala1144=
ENST00000578373.5:c.*3267T>C	ENSP00000463427.1:n.*3267T>C
ENST00000584450.5:c.*56T>C	ENSP00000463714.1:n.*56T>C
ENST00000584601.5:c.3387T>C	ENSP00000462438.1:p.Ala1129=
NM_001005862.2:c.3387T>C , LRG_724t1:c.3387T>C	NP_001005862.1:p.Ala1129=
NM_001289936.1:c.3432T>C , LRG_724t4:c.3432T>C	NP_001276865.1:p.Ala1144=
NM_001289937.1:c.*56T>C	NP_001276866.1:n.*56T>C
NM_004448.3:c.3477T>C , LRG_724t2:c.3477T>C	NP_004439.2:p.Ala1159=
NR_110535.1:n.3801T>C
XM_024450641.1:c.3615T>C	XP_024306409.1:p.Ala1205=
XM_024450642.1:c.3570T>C	XP_024306410.1:p.Ala1190=
XM_024450643.1:c.3525T>C	XP_024306411.1:p.Ala1175=
NM_001005862.3:c.3387T>C	NP_001005862.1:p.Ala1129=
NM_001289936.2:c.3432T>C	NP_001276865.1:p.Ala1144=
NM_001289937.2:c.*56T>C	NP_001276866.1:n.*56T>C
NM_001382782.1:c.3387T>C	NP_001369711.1:p.Ala1129=
NM_001382783.1:c.3387T>C	NP_001369712.1:p.Ala1129=
NM_001382784.1:c.3594T>C	NP_001369713.1:p.Ala1198=
NM_001382785.1:c.3579T>C	NP_001369714.1:p.Ala1193=
NM_001382786.1:c.3558T>C	NP_001369715.1:p.Ala1186=
NM_001382787.1:c.3552T>C	NP_001369716.1:p.Ala1184=
NM_001382788.1:c.3507T>C	NP_001369717.1:p.Ala1169=
NM_001382789.1:c.3498T>C	NP_001369718.1:p.Ala1166=
NM_001382790.1:c.3474T>C	NP_001369719.1:p.Ala1158=
NM_001382791.1:c.3468T>C	NP_001369720.1:p.Ala1156=
NM_001382792.1:c.3441T>C	NP_001369721.1:p.Ala1147=
NM_001382793.1:c.3435T>C	NP_001369722.1:p.Ala1145=
NM_001382794.1:c.3435T>C	NP_001369723.1:p.Ala1145=
NM_001382795.1:c.3429T>C	NP_001369724.1:p.Ala1143=
NM_001382796.1:c.3390T>C	NP_001369725.1:p.Ala1130=
NM_001382797.1:c.3378T>C	NP_001369726.1:p.Ala1126=
NM_001382798.1:c.3321T>C	NP_001369727.1:p.Ala1107=
NM_001382799.1:c.3297T>C	NP_001369728.1:p.Ala1099=
NM_001382800.1:c.3291T>C	NP_001369729.1:p.Ala1097=
NM_001382801.1:c.3273T>C	NP_001369730.1:p.Ala1091=
NM_001382802.1:c.3219T>C	NP_001369731.1:p.Ala1073=
NM_001382803.1:c.*56T>C	NP_001369732.1:n.*56T>C
NM_001382804.1:c.2649T>C	NP_001369733.1:p.Ala883=
NM_001382805.1:c.2526T>C	NP_001369734.1:p.Ala842=
NM_001382806.1:c.2439T>C	NP_001369735.1:p.Ala813=
NM_004448.4:c.3477T>C MANE Select	NP_004439.2:p.Ala1159=
NR_110535.2:n.3715T>C