Canonical Allele Identifier: CA399312891

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143289735
• MyVariant Identifiers: chr17:g.37883975C>G (hg19) ; chr17:g.39727722C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727722C>G , CM000679.2:g.39727722C>G	GRCh38
NC_000017.10:g.37883975C>G , CM000679.1:g.37883975C>G	GRCh37
NC_000017.9:g.35137501C>G	NCBI36
NG_007503.1:g.44583C>G , LRG_724:g.44583C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3446C>G MANE Select	ENSP00000269571.4:p.Pro1149Arg
ENST00000269571.9:c.3446C>G	ENSP00000269571.4:p.Pro1149Arg
ENST00000406381.6:c.3356C>G	ENSP00000385185.2:p.Pro1119Arg
ENST00000445658.6:c.2618C>G	ENSP00000404047.2:p.Pro873Arg
ENST00000541774.5:c.3401C>G	ENSP00000446466.1:p.Pro1134Arg
ENST00000578373.5:c.*3236C>G	ENSP00000463427.1:n.*3236C>G
ENST00000584450.5:c.*25C>G	ENSP00000463714.1:n.*25C>G
ENST00000584601.5:c.3356C>G	ENSP00000462438.1:p.Pro1119Arg
NM_001005862.2:c.3356C>G , LRG_724t1:c.3356C>G	NP_001005862.1:p.Pro1119Arg
NM_001289936.1:c.3401C>G , LRG_724t4:c.3401C>G	NP_001276865.1:p.Pro1134Arg
NM_001289937.1:c.*25C>G	NP_001276866.1:n.*25C>G
NM_004448.3:c.3446C>G , LRG_724t2:c.3446C>G	NP_004439.2:p.Pro1149Arg
NR_110535.1:n.3770C>G
XM_024450641.1:c.3584C>G	XP_024306409.1:p.Pro1195Arg
XM_024450642.1:c.3539C>G	XP_024306410.1:p.Pro1180Arg
XM_024450643.1:c.3494C>G	XP_024306411.1:p.Pro1165Arg
NM_001005862.3:c.3356C>G	NP_001005862.1:p.Pro1119Arg
NM_001289936.2:c.3401C>G	NP_001276865.1:p.Pro1134Arg
NM_001289937.2:c.*25C>G	NP_001276866.1:n.*25C>G
NM_001382782.1:c.3356C>G	NP_001369711.1:p.Pro1119Arg
NM_001382783.1:c.3356C>G	NP_001369712.1:p.Pro1119Arg
NM_001382784.1:c.3563C>G	NP_001369713.1:p.Pro1188Arg
NM_001382785.1:c.3548C>G	NP_001369714.1:p.Pro1183Arg
NM_001382786.1:c.3527C>G	NP_001369715.1:p.Pro1176Arg
NM_001382787.1:c.3521C>G	NP_001369716.1:p.Pro1174Arg
NM_001382788.1:c.3476C>G	NP_001369717.1:p.Pro1159Arg
NM_001382789.1:c.3467C>G	NP_001369718.1:p.Pro1156Arg
NM_001382790.1:c.3443C>G	NP_001369719.1:p.Pro1148Arg
NM_001382791.1:c.3437C>G	NP_001369720.1:p.Pro1146Arg
NM_001382792.1:c.3410C>G	NP_001369721.1:p.Pro1137Arg
NM_001382793.1:c.3404C>G	NP_001369722.1:p.Pro1135Arg
NM_001382794.1:c.3404C>G	NP_001369723.1:p.Pro1135Arg
NM_001382795.1:c.3398C>G	NP_001369724.1:p.Pro1133Arg
NM_001382796.1:c.3359C>G	NP_001369725.1:p.Pro1120Arg
NM_001382797.1:c.3347C>G	NP_001369726.1:p.Pro1116Arg
NM_001382798.1:c.3290C>G	NP_001369727.1:p.Pro1097Arg
NM_001382799.1:c.3266C>G	NP_001369728.1:p.Pro1089Arg
NM_001382800.1:c.3260C>G	NP_001369729.1:p.Pro1087Arg
NM_001382801.1:c.3242C>G	NP_001369730.1:p.Pro1081Arg
NM_001382802.1:c.3188C>G	NP_001369731.1:p.Pro1063Arg
NM_001382803.1:c.*25C>G	NP_001369732.1:n.*25C>G
NM_001382804.1:c.2618C>G	NP_001369733.1:p.Pro873Arg
NM_001382805.1:c.2495C>G	NP_001369734.1:p.Pro832Arg
NM_001382806.1:c.2408C>G	NP_001369735.1:p.Pro803Arg
NM_004448.4:c.3446C>G MANE Select	NP_004439.2:p.Pro1149Arg
NR_110535.2:n.3684C>G