Canonical Allele Identifier: CA499890263

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883745C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727492C>A , CM000679.2:g.39727492C>A	GRCh38
NC_000017.10:g.37883745C>A , CM000679.1:g.37883745C>A	GRCh37
NC_000017.9:g.35137271C>A	NCBI36
NG_007503.1:g.44353C>A , LRG_724:g.44353C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3357C>A MANE Select	ENSP00000269571.4:p.Pro1119=
ENST00000269571.9:c.3357C>A	ENSP00000269571.4:p.Pro1119=
ENST00000406381.6:c.3267C>A	ENSP00000385185.2:p.Pro1089=
ENST00000445658.6:c.2529C>A	ENSP00000404047.2:p.Pro843=
ENST00000541774.5:c.3312C>A	ENSP00000446466.1:p.Pro1104=
ENST00000578373.5:c.*3147C>A	ENSP00000463427.1:n.*3147C>A
ENST00000584450.5:c.3160-197C>A	ENSP00000463714.1:n.3160-197C>A
ENST00000584601.5:c.3267C>A	ENSP00000462438.1:p.Pro1089=
NM_001005862.2:c.3267C>A , LRG_724t1:c.3267C>A	NP_001005862.1:p.Pro1089=
NM_001289936.1:c.3312C>A , LRG_724t4:c.3312C>A	NP_001276865.1:p.Pro1104=
NM_001289937.1:c.3160-197C>A	NP_001276866.1:n.3160-197C>A
NM_004448.3:c.3357C>A , LRG_724t2:c.3357C>A	NP_004439.2:p.Pro1119=
NR_110535.1:n.3681C>A
XM_024450641.1:c.3495C>A	XP_024306409.1:p.Pro1165=
XM_024450642.1:c.3450C>A	XP_024306410.1:p.Pro1150=
XM_024450643.1:c.3405C>A	XP_024306411.1:p.Pro1135=
NM_001005862.3:c.3267C>A	NP_001005862.1:p.Pro1089=
NM_001289936.2:c.3312C>A	NP_001276865.1:p.Pro1104=
NM_001289937.2:c.3160-197C>A	NP_001276866.1:n.3160-197C>A
NM_001382782.1:c.3267C>A	NP_001369711.1:p.Pro1089=
NM_001382783.1:c.3267C>A	NP_001369712.1:p.Pro1089=
NM_001382784.1:c.3474C>A	NP_001369713.1:p.Pro1158=
NM_001382785.1:c.3459C>A	NP_001369714.1:p.Pro1153=
NM_001382786.1:c.3438C>A	NP_001369715.1:p.Pro1146=
NM_001382787.1:c.3432C>A	NP_001369716.1:p.Pro1144=
NM_001382788.1:c.3387C>A	NP_001369717.1:p.Pro1129=
NM_001382789.1:c.3378C>A	NP_001369718.1:p.Pro1126=
NM_001382790.1:c.3354C>A	NP_001369719.1:p.Pro1118=
NM_001382791.1:c.3348C>A	NP_001369720.1:p.Pro1116=
NM_001382792.1:c.3321C>A	NP_001369721.1:p.Pro1107=
NM_001382793.1:c.3315C>A	NP_001369722.1:p.Pro1105=
NM_001382794.1:c.3315C>A	NP_001369723.1:p.Pro1105=
NM_001382795.1:c.3309C>A	NP_001369724.1:p.Pro1103=
NM_001382796.1:c.3270C>A	NP_001369725.1:p.Pro1090=
NM_001382797.1:c.3258C>A	NP_001369726.1:p.Pro1086=
NM_001382798.1:c.3201C>A	NP_001369727.1:p.Pro1067=
NM_001382799.1:c.3177C>A	NP_001369728.1:p.Pro1059=
NM_001382800.1:c.3171C>A	NP_001369729.1:p.Pro1057=
NM_001382801.1:c.3153C>A	NP_001369730.1:p.Pro1051=
NM_001382802.1:c.3099C>A	NP_001369731.1:p.Pro1033=
NM_001382803.1:c.3118-197C>A	NP_001369732.1:n.3118-197C>A
NM_001382804.1:c.2529C>A	NP_001369733.1:p.Pro843=
NM_001382805.1:c.2406C>A	NP_001369734.1:p.Pro802=
NM_001382806.1:c.2319C>A	NP_001369735.1:p.Pro773=
NM_004448.4:c.3357C>A MANE Select	NP_004439.2:p.Pro1119=
NR_110535.2:n.3595C>A