Canonical Allele Identifier: CA499890823

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884156T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727903T>C , CM000679.2:g.39727903T>C	GRCh38
NC_000017.10:g.37884156T>C , CM000679.1:g.37884156T>C	GRCh37
NC_000017.9:g.35137682T>C	NCBI36
NG_007503.1:g.44764T>C , LRG_724:g.44764T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3627T>C MANE Select	ENSP00000269571.4:p.Pro1209=
ENST00000269571.9:c.3627T>C	ENSP00000269571.4:p.Pro1209=
ENST00000406381.6:c.3537T>C	ENSP00000385185.2:p.Pro1179=
ENST00000445658.6:c.2799T>C	ENSP00000404047.2:p.Pro933=
ENST00000541774.5:c.3582T>C	ENSP00000446466.1:p.Pro1194=
ENST00000578373.5:c.*3417T>C	ENSP00000463427.1:n.*3417T>C
ENST00000584450.5:c.*206T>C	ENSP00000463714.1:n.*206T>C
ENST00000584601.5:c.3537T>C	ENSP00000462438.1:p.Pro1179=
NM_001005862.2:c.3537T>C , LRG_724t1:c.3537T>C	NP_001005862.1:p.Pro1179=
NM_001289936.1:c.3582T>C , LRG_724t4:c.3582T>C	NP_001276865.1:p.Pro1194=
NM_001289937.1:c.*206T>C	NP_001276866.1:n.*206T>C
NM_004448.3:c.3627T>C , LRG_724t2:c.3627T>C	NP_004439.2:p.Pro1209=
NR_110535.1:n.3951T>C
XM_024450641.1:c.3765T>C	XP_024306409.1:p.Pro1255=
XM_024450642.1:c.3720T>C	XP_024306410.1:p.Pro1240=
XM_024450643.1:c.3675T>C	XP_024306411.1:p.Pro1225=
NM_001005862.3:c.3537T>C	NP_001005862.1:p.Pro1179=
NM_001289936.2:c.3582T>C	NP_001276865.1:p.Pro1194=
NM_001289937.2:c.*206T>C	NP_001276866.1:n.*206T>C
NM_001382782.1:c.3537T>C	NP_001369711.1:p.Pro1179=
NM_001382783.1:c.3537T>C	NP_001369712.1:p.Pro1179=
NM_001382784.1:c.3744T>C	NP_001369713.1:p.Pro1248=
NM_001382785.1:c.3729T>C	NP_001369714.1:p.Pro1243=
NM_001382786.1:c.3708T>C	NP_001369715.1:p.Pro1236=
NM_001382787.1:c.3702T>C	NP_001369716.1:p.Pro1234=
NM_001382788.1:c.3657T>C	NP_001369717.1:p.Pro1219=
NM_001382789.1:c.3648T>C	NP_001369718.1:p.Pro1216=
NM_001382790.1:c.3624T>C	NP_001369719.1:p.Pro1208=
NM_001382791.1:c.3618T>C	NP_001369720.1:p.Pro1206=
NM_001382792.1:c.3591T>C	NP_001369721.1:p.Pro1197=
NM_001382793.1:c.3585T>C	NP_001369722.1:p.Pro1195=
NM_001382794.1:c.3585T>C	NP_001369723.1:p.Pro1195=
NM_001382795.1:c.3579T>C	NP_001369724.1:p.Pro1193=
NM_001382796.1:c.3540T>C	NP_001369725.1:p.Pro1180=
NM_001382797.1:c.3528T>C	NP_001369726.1:p.Pro1176=
NM_001382798.1:c.3471T>C	NP_001369727.1:p.Pro1157=
NM_001382799.1:c.3447T>C	NP_001369728.1:p.Pro1149=
NM_001382800.1:c.3441T>C	NP_001369729.1:p.Pro1147=
NM_001382801.1:c.3423T>C	NP_001369730.1:p.Pro1141=
NM_001382802.1:c.3369T>C	NP_001369731.1:p.Pro1123=
NM_001382803.1:c.*206T>C	NP_001369732.1:n.*206T>C
NM_001382804.1:c.2799T>C	NP_001369733.1:p.Pro933=
NM_001382805.1:c.2676T>C	NP_001369734.1:p.Pro892=
NM_001382806.1:c.2589T>C	NP_001369735.1:p.Pro863=
NM_004448.4:c.3627T>C MANE Select	NP_004439.2:p.Pro1209=
NR_110535.2:n.3865T>C