Canonical Allele Identifier: CA399313283

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884049T>C (hg19) ; chr17:g.39727796T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727796T>C , CM000679.2:g.39727796T>C	GRCh38
NC_000017.10:g.37884049T>C , CM000679.1:g.37884049T>C	GRCh37
NC_000017.9:g.35137575T>C	NCBI36
NG_007503.1:g.44657T>C , LRG_724:g.44657T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3520T>C MANE Select	ENSP00000269571.4:p.Ser1174Pro
ENST00000269571.9:c.3520T>C	ENSP00000269571.4:p.Ser1174Pro
ENST00000406381.6:c.3430T>C	ENSP00000385185.2:p.Ser1144Pro
ENST00000445658.6:c.2692T>C	ENSP00000404047.2:p.Ser898Pro
ENST00000541774.5:c.3475T>C	ENSP00000446466.1:p.Ser1159Pro
ENST00000578373.5:c.*3310T>C	ENSP00000463427.1:n.*3310T>C
ENST00000584450.5:c.*99T>C	ENSP00000463714.1:n.*99T>C
ENST00000584601.5:c.3430T>C	ENSP00000462438.1:p.Ser1144Pro
NM_001005862.2:c.3430T>C , LRG_724t1:c.3430T>C	NP_001005862.1:p.Ser1144Pro
NM_001289936.1:c.3475T>C , LRG_724t4:c.3475T>C	NP_001276865.1:p.Ser1159Pro
NM_001289937.1:c.*99T>C	NP_001276866.1:n.*99T>C
NM_004448.3:c.3520T>C , LRG_724t2:c.3520T>C	NP_004439.2:p.Ser1174Pro
NR_110535.1:n.3844T>C
XM_024450641.1:c.3658T>C	XP_024306409.1:p.Ser1220Pro
XM_024450642.1:c.3613T>C	XP_024306410.1:p.Ser1205Pro
XM_024450643.1:c.3568T>C	XP_024306411.1:p.Ser1190Pro
NM_001005862.3:c.3430T>C	NP_001005862.1:p.Ser1144Pro
NM_001289936.2:c.3475T>C	NP_001276865.1:p.Ser1159Pro
NM_001289937.2:c.*99T>C	NP_001276866.1:n.*99T>C
NM_001382782.1:c.3430T>C	NP_001369711.1:p.Ser1144Pro
NM_001382783.1:c.3430T>C	NP_001369712.1:p.Ser1144Pro
NM_001382784.1:c.3637T>C	NP_001369713.1:p.Ser1213Pro
NM_001382785.1:c.3622T>C	NP_001369714.1:p.Ser1208Pro
NM_001382786.1:c.3601T>C	NP_001369715.1:p.Ser1201Pro
NM_001382787.1:c.3595T>C	NP_001369716.1:p.Ser1199Pro
NM_001382788.1:c.3550T>C	NP_001369717.1:p.Ser1184Pro
NM_001382789.1:c.3541T>C	NP_001369718.1:p.Ser1181Pro
NM_001382790.1:c.3517T>C	NP_001369719.1:p.Ser1173Pro
NM_001382791.1:c.3511T>C	NP_001369720.1:p.Ser1171Pro
NM_001382792.1:c.3484T>C	NP_001369721.1:p.Ser1162Pro
NM_001382793.1:c.3478T>C	NP_001369722.1:p.Ser1160Pro
NM_001382794.1:c.3478T>C	NP_001369723.1:p.Ser1160Pro
NM_001382795.1:c.3472T>C	NP_001369724.1:p.Ser1158Pro
NM_001382796.1:c.3433T>C	NP_001369725.1:p.Ser1145Pro
NM_001382797.1:c.3421T>C	NP_001369726.1:p.Ser1141Pro
NM_001382798.1:c.3364T>C	NP_001369727.1:p.Ser1122Pro
NM_001382799.1:c.3340T>C	NP_001369728.1:p.Ser1114Pro
NM_001382800.1:c.3334T>C	NP_001369729.1:p.Ser1112Pro
NM_001382801.1:c.3316T>C	NP_001369730.1:p.Ser1106Pro
NM_001382802.1:c.3262T>C	NP_001369731.1:p.Ser1088Pro
NM_001382803.1:c.*99T>C	NP_001369732.1:n.*99T>C
NM_001382804.1:c.2692T>C	NP_001369733.1:p.Ser898Pro
NM_001382805.1:c.2569T>C	NP_001369734.1:p.Ser857Pro
NM_001382806.1:c.2482T>C	NP_001369735.1:p.Ser828Pro
NM_004448.4:c.3520T>C MANE Select	NP_004439.2:p.Ser1174Pro
NR_110535.2:n.3758T>C