Canonical Allele Identifier: CA399312947

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883996C>G (hg19) ; chr17:g.39727743C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727743C>G , CM000679.2:g.39727743C>G	GRCh38
NC_000017.10:g.37883996C>G , CM000679.1:g.37883996C>G	GRCh37
NC_000017.9:g.35137522C>G	NCBI36
NG_007503.1:g.44604C>G , LRG_724:g.44604C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3467C>G MANE Select	ENSP00000269571.4:p.Pro1156Arg
ENST00000269571.9:c.3467C>G	ENSP00000269571.4:p.Pro1156Arg
ENST00000406381.6:c.3377C>G	ENSP00000385185.2:p.Pro1126Arg
ENST00000445658.6:c.2639C>G	ENSP00000404047.2:p.Pro880Arg
ENST00000541774.5:c.3422C>G	ENSP00000446466.1:p.Pro1141Arg
ENST00000578373.5:c.*3257C>G	ENSP00000463427.1:n.*3257C>G
ENST00000584450.5:c.*46C>G	ENSP00000463714.1:n.*46C>G
ENST00000584601.5:c.3377C>G	ENSP00000462438.1:p.Pro1126Arg
NM_001005862.2:c.3377C>G , LRG_724t1:c.3377C>G	NP_001005862.1:p.Pro1126Arg
NM_001289936.1:c.3422C>G , LRG_724t4:c.3422C>G	NP_001276865.1:p.Pro1141Arg
NM_001289937.1:c.*46C>G	NP_001276866.1:n.*46C>G
NM_004448.3:c.3467C>G , LRG_724t2:c.3467C>G	NP_004439.2:p.Pro1156Arg
NR_110535.1:n.3791C>G
XM_024450641.1:c.3605C>G	XP_024306409.1:p.Pro1202Arg
XM_024450642.1:c.3560C>G	XP_024306410.1:p.Pro1187Arg
XM_024450643.1:c.3515C>G	XP_024306411.1:p.Pro1172Arg
NM_001005862.3:c.3377C>G	NP_001005862.1:p.Pro1126Arg
NM_001289936.2:c.3422C>G	NP_001276865.1:p.Pro1141Arg
NM_001289937.2:c.*46C>G	NP_001276866.1:n.*46C>G
NM_001382782.1:c.3377C>G	NP_001369711.1:p.Pro1126Arg
NM_001382783.1:c.3377C>G	NP_001369712.1:p.Pro1126Arg
NM_001382784.1:c.3584C>G	NP_001369713.1:p.Pro1195Arg
NM_001382785.1:c.3569C>G	NP_001369714.1:p.Pro1190Arg
NM_001382786.1:c.3548C>G	NP_001369715.1:p.Pro1183Arg
NM_001382787.1:c.3542C>G	NP_001369716.1:p.Pro1181Arg
NM_001382788.1:c.3497C>G	NP_001369717.1:p.Pro1166Arg
NM_001382789.1:c.3488C>G	NP_001369718.1:p.Pro1163Arg
NM_001382790.1:c.3464C>G	NP_001369719.1:p.Pro1155Arg
NM_001382791.1:c.3458C>G	NP_001369720.1:p.Pro1153Arg
NM_001382792.1:c.3431C>G	NP_001369721.1:p.Pro1144Arg
NM_001382793.1:c.3425C>G	NP_001369722.1:p.Pro1142Arg
NM_001382794.1:c.3425C>G	NP_001369723.1:p.Pro1142Arg
NM_001382795.1:c.3419C>G	NP_001369724.1:p.Pro1140Arg
NM_001382796.1:c.3380C>G	NP_001369725.1:p.Pro1127Arg
NM_001382797.1:c.3368C>G	NP_001369726.1:p.Pro1123Arg
NM_001382798.1:c.3311C>G	NP_001369727.1:p.Pro1104Arg
NM_001382799.1:c.3287C>G	NP_001369728.1:p.Pro1096Arg
NM_001382800.1:c.3281C>G	NP_001369729.1:p.Pro1094Arg
NM_001382801.1:c.3263C>G	NP_001369730.1:p.Pro1088Arg
NM_001382802.1:c.3209C>G	NP_001369731.1:p.Pro1070Arg
NM_001382803.1:c.*46C>G	NP_001369732.1:n.*46C>G
NM_001382804.1:c.2639C>G	NP_001369733.1:p.Pro880Arg
NM_001382805.1:c.2516C>G	NP_001369734.1:p.Pro839Arg
NM_001382806.1:c.2429C>G	NP_001369735.1:p.Pro810Arg
NM_004448.4:c.3467C>G MANE Select	NP_004439.2:p.Pro1156Arg
NR_110535.2:n.3705C>G