Canonical Allele Identifier: CA399310893

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39727439-C-G
• MyVariant Identifiers: chr17:g.37883692C>G (hg19) ; chr17:g.39727439C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727439C>G , CM000679.2:g.39727439C>G	GRCh38
NC_000017.10:g.37883692C>G , CM000679.1:g.37883692C>G	GRCh37
NC_000017.9:g.35137218C>G	NCBI36
NG_007503.1:g.44300C>G , LRG_724:g.44300C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3304C>G MANE Select	ENSP00000269571.4:p.Pro1102Ala
ENST00000269571.9:c.3304C>G	ENSP00000269571.4:p.Pro1102Ala
ENST00000406381.6:c.3214C>G	ENSP00000385185.2:p.Pro1072Ala
ENST00000445658.6:c.2476C>G	ENSP00000404047.2:p.Pro826Ala
ENST00000541774.5:c.3259C>G	ENSP00000446466.1:p.Pro1087Ala
ENST00000578373.5:c.*3094C>G	ENSP00000463427.1:n.*3094C>G
ENST00000584450.5:c.3160-250C>G	ENSP00000463714.1:n.3160-250C>G
ENST00000584601.5:c.3214C>G	ENSP00000462438.1:p.Pro1072Ala
NM_001005862.2:c.3214C>G , LRG_724t1:c.3214C>G	NP_001005862.1:p.Pro1072Ala
NM_001289936.1:c.3259C>G , LRG_724t4:c.3259C>G	NP_001276865.1:p.Pro1087Ala
NM_001289937.1:c.3160-250C>G	NP_001276866.1:n.3160-250C>G
NM_004448.3:c.3304C>G , LRG_724t2:c.3304C>G	NP_004439.2:p.Pro1102Ala
NR_110535.1:n.3628C>G
XM_024450641.1:c.3442C>G	XP_024306409.1:p.Pro1148Ala
XM_024450642.1:c.3397C>G	XP_024306410.1:p.Pro1133Ala
XM_024450643.1:c.3352C>G	XP_024306411.1:p.Pro1118Ala
NM_001005862.3:c.3214C>G	NP_001005862.1:p.Pro1072Ala
NM_001289936.2:c.3259C>G	NP_001276865.1:p.Pro1087Ala
NM_001289937.2:c.3160-250C>G	NP_001276866.1:n.3160-250C>G
NM_001382782.1:c.3214C>G	NP_001369711.1:p.Pro1072Ala
NM_001382783.1:c.3214C>G	NP_001369712.1:p.Pro1072Ala
NM_001382784.1:c.3421C>G	NP_001369713.1:p.Pro1141Ala
NM_001382785.1:c.3406C>G	NP_001369714.1:p.Pro1136Ala
NM_001382786.1:c.3385C>G	NP_001369715.1:p.Pro1129Ala
NM_001382787.1:c.3379C>G	NP_001369716.1:p.Pro1127Ala
NM_001382788.1:c.3334C>G	NP_001369717.1:p.Pro1112Ala
NM_001382789.1:c.3325C>G	NP_001369718.1:p.Pro1109Ala
NM_001382790.1:c.3301C>G	NP_001369719.1:p.Pro1101Ala
NM_001382791.1:c.3295C>G	NP_001369720.1:p.Pro1099Ala
NM_001382792.1:c.3268C>G	NP_001369721.1:p.Pro1090Ala
NM_001382793.1:c.3262C>G	NP_001369722.1:p.Pro1088Ala
NM_001382794.1:c.3262C>G	NP_001369723.1:p.Pro1088Ala
NM_001382795.1:c.3256C>G	NP_001369724.1:p.Pro1086Ala
NM_001382796.1:c.3217C>G	NP_001369725.1:p.Pro1073Ala
NM_001382797.1:c.3205C>G	NP_001369726.1:p.Pro1069Ala
NM_001382798.1:c.3148C>G	NP_001369727.1:p.Pro1050Ala
NM_001382799.1:c.3124C>G	NP_001369728.1:p.Pro1042Ala
NM_001382800.1:c.3118C>G	NP_001369729.1:p.Pro1040Ala
NM_001382801.1:c.3100C>G	NP_001369730.1:p.Pro1034Ala
NM_001382802.1:c.3046C>G	NP_001369731.1:p.Pro1016Ala
NM_001382803.1:c.3118-250C>G	NP_001369732.1:n.3118-250C>G
NM_001382804.1:c.2476C>G	NP_001369733.1:p.Pro826Ala
NM_001382805.1:c.2353C>G	NP_001369734.1:p.Pro785Ala
NM_001382806.1:c.2266C>G	NP_001369735.1:p.Pro756Ala
NM_004448.4:c.3304C>G MANE Select	NP_004439.2:p.Pro1102Ala
NR_110535.2:n.3542C>G