Canonical Allele Identifier: CA499890700

Gene: ERBB2

Linked Data

• dbSNP Id: rs1411350560
• MyVariant Identifiers: chr17:g.37884054A>C (hg19) ; chr17:g.39727801A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727801A>C , CM000679.2:g.39727801A>C	GRCh38
NC_000017.10:g.37884054A>C , CM000679.1:g.37884054A>C	GRCh37
NC_000017.9:g.35137580A>C	NCBI36
NG_007503.1:g.44662A>C , LRG_724:g.44662A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3525A>C MANE Select	ENSP00000269571.4:p.Pro1175=
ENST00000269571.9:c.3525A>C	ENSP00000269571.4:p.Pro1175=
ENST00000406381.6:c.3435A>C	ENSP00000385185.2:p.Pro1145=
ENST00000445658.6:c.2697A>C	ENSP00000404047.2:p.Pro899=
ENST00000541774.5:c.3480A>C	ENSP00000446466.1:p.Pro1160=
ENST00000578373.5:c.*3315A>C	ENSP00000463427.1:n.*3315A>C
ENST00000584450.5:c.*104A>C	ENSP00000463714.1:n.*104A>C
ENST00000584601.5:c.3435A>C	ENSP00000462438.1:p.Pro1145=
NM_001005862.2:c.3435A>C , LRG_724t1:c.3435A>C	NP_001005862.1:p.Pro1145=
NM_001289936.1:c.3480A>C , LRG_724t4:c.3480A>C	NP_001276865.1:p.Pro1160=
NM_001289937.1:c.*104A>C	NP_001276866.1:n.*104A>C
NM_004448.3:c.3525A>C , LRG_724t2:c.3525A>C	NP_004439.2:p.Pro1175=
NR_110535.1:n.3849A>C
XM_024450641.1:c.3663A>C	XP_024306409.1:p.Pro1221=
XM_024450642.1:c.3618A>C	XP_024306410.1:p.Pro1206=
XM_024450643.1:c.3573A>C	XP_024306411.1:p.Pro1191=
NM_001005862.3:c.3435A>C	NP_001005862.1:p.Pro1145=
NM_001289936.2:c.3480A>C	NP_001276865.1:p.Pro1160=
NM_001289937.2:c.*104A>C	NP_001276866.1:n.*104A>C
NM_001382782.1:c.3435A>C	NP_001369711.1:p.Pro1145=
NM_001382783.1:c.3435A>C	NP_001369712.1:p.Pro1145=
NM_001382784.1:c.3642A>C	NP_001369713.1:p.Pro1214=
NM_001382785.1:c.3627A>C	NP_001369714.1:p.Pro1209=
NM_001382786.1:c.3606A>C	NP_001369715.1:p.Pro1202=
NM_001382787.1:c.3600A>C	NP_001369716.1:p.Pro1200=
NM_001382788.1:c.3555A>C	NP_001369717.1:p.Pro1185=
NM_001382789.1:c.3546A>C	NP_001369718.1:p.Pro1182=
NM_001382790.1:c.3522A>C	NP_001369719.1:p.Pro1174=
NM_001382791.1:c.3516A>C	NP_001369720.1:p.Pro1172=
NM_001382792.1:c.3489A>C	NP_001369721.1:p.Pro1163=
NM_001382793.1:c.3483A>C	NP_001369722.1:p.Pro1161=
NM_001382794.1:c.3483A>C	NP_001369723.1:p.Pro1161=
NM_001382795.1:c.3477A>C	NP_001369724.1:p.Pro1159=
NM_001382796.1:c.3438A>C	NP_001369725.1:p.Pro1146=
NM_001382797.1:c.3426A>C	NP_001369726.1:p.Pro1142=
NM_001382798.1:c.3369A>C	NP_001369727.1:p.Pro1123=
NM_001382799.1:c.3345A>C	NP_001369728.1:p.Pro1115=
NM_001382800.1:c.3339A>C	NP_001369729.1:p.Pro1113=
NM_001382801.1:c.3321A>C	NP_001369730.1:p.Pro1107=
NM_001382802.1:c.3267A>C	NP_001369731.1:p.Pro1089=
NM_001382803.1:c.*104A>C	NP_001369732.1:n.*104A>C
NM_001382804.1:c.2697A>C	NP_001369733.1:p.Pro899=
NM_001382805.1:c.2574A>C	NP_001369734.1:p.Pro858=
NM_001382806.1:c.2487A>C	NP_001369735.1:p.Pro829=
NM_004448.4:c.3525A>C MANE Select	NP_004439.2:p.Pro1175=
NR_110535.2:n.3763A>C