Canonical Allele Identifier: CA399312909

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143290777
• MyVariant Identifiers: chr17:g.37883984C>T (hg19) ; chr17:g.39727731C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727731C>T , CM000679.2:g.39727731C>T	GRCh38
NC_000017.10:g.37883984C>T , CM000679.1:g.37883984C>T	GRCh37
NC_000017.9:g.35137510C>T	NCBI36
NG_007503.1:g.44592C>T , LRG_724:g.44592C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3455C>T MANE Select	ENSP00000269571.4:p.Pro1152Leu
ENST00000269571.9:c.3455C>T	ENSP00000269571.4:p.Pro1152Leu
ENST00000406381.6:c.3365C>T	ENSP00000385185.2:p.Pro1122Leu
ENST00000445658.6:c.2627C>T	ENSP00000404047.2:p.Pro876Leu
ENST00000541774.5:c.3410C>T	ENSP00000446466.1:p.Pro1137Leu
ENST00000578373.5:c.*3245C>T	ENSP00000463427.1:n.*3245C>T
ENST00000584450.5:c.*34C>T	ENSP00000463714.1:n.*34C>T
ENST00000584601.5:c.3365C>T	ENSP00000462438.1:p.Pro1122Leu
NM_001005862.2:c.3365C>T , LRG_724t1:c.3365C>T	NP_001005862.1:p.Pro1122Leu
NM_001289936.1:c.3410C>T , LRG_724t4:c.3410C>T	NP_001276865.1:p.Pro1137Leu
NM_001289937.1:c.*34C>T	NP_001276866.1:n.*34C>T
NM_004448.3:c.3455C>T , LRG_724t2:c.3455C>T	NP_004439.2:p.Pro1152Leu
NR_110535.1:n.3779C>T
XM_024450641.1:c.3593C>T	XP_024306409.1:p.Pro1198Leu
XM_024450642.1:c.3548C>T	XP_024306410.1:p.Pro1183Leu
XM_024450643.1:c.3503C>T	XP_024306411.1:p.Pro1168Leu
NM_001005862.3:c.3365C>T	NP_001005862.1:p.Pro1122Leu
NM_001289936.2:c.3410C>T	NP_001276865.1:p.Pro1137Leu
NM_001289937.2:c.*34C>T	NP_001276866.1:n.*34C>T
NM_001382782.1:c.3365C>T	NP_001369711.1:p.Pro1122Leu
NM_001382783.1:c.3365C>T	NP_001369712.1:p.Pro1122Leu
NM_001382784.1:c.3572C>T	NP_001369713.1:p.Pro1191Leu
NM_001382785.1:c.3557C>T	NP_001369714.1:p.Pro1186Leu
NM_001382786.1:c.3536C>T	NP_001369715.1:p.Pro1179Leu
NM_001382787.1:c.3530C>T	NP_001369716.1:p.Pro1177Leu
NM_001382788.1:c.3485C>T	NP_001369717.1:p.Pro1162Leu
NM_001382789.1:c.3476C>T	NP_001369718.1:p.Pro1159Leu
NM_001382790.1:c.3452C>T	NP_001369719.1:p.Pro1151Leu
NM_001382791.1:c.3446C>T	NP_001369720.1:p.Pro1149Leu
NM_001382792.1:c.3419C>T	NP_001369721.1:p.Pro1140Leu
NM_001382793.1:c.3413C>T	NP_001369722.1:p.Pro1138Leu
NM_001382794.1:c.3413C>T	NP_001369723.1:p.Pro1138Leu
NM_001382795.1:c.3407C>T	NP_001369724.1:p.Pro1136Leu
NM_001382796.1:c.3368C>T	NP_001369725.1:p.Pro1123Leu
NM_001382797.1:c.3356C>T	NP_001369726.1:p.Pro1119Leu
NM_001382798.1:c.3299C>T	NP_001369727.1:p.Pro1100Leu
NM_001382799.1:c.3275C>T	NP_001369728.1:p.Pro1092Leu
NM_001382800.1:c.3269C>T	NP_001369729.1:p.Pro1090Leu
NM_001382801.1:c.3251C>T	NP_001369730.1:p.Pro1084Leu
NM_001382802.1:c.3197C>T	NP_001369731.1:p.Pro1066Leu
NM_001382803.1:c.*34C>T	NP_001369732.1:n.*34C>T
NM_001382804.1:c.2627C>T	NP_001369733.1:p.Pro876Leu
NM_001382805.1:c.2504C>T	NP_001369734.1:p.Pro835Leu
NM_001382806.1:c.2417C>T	NP_001369735.1:p.Pro806Leu
NM_004448.4:c.3455C>T MANE Select	NP_004439.2:p.Pro1152Leu
NR_110535.2:n.3693C>T