Canonical Allele Identifier: CA290443774

Gene: ERBB2

Linked Data

• dbSNP Id: rs562773948
• gnomAD v3: 17-39727724-C-G
• gnomAD v4: 17-39727724-C-G
• MyVariant Identifiers: chr17:g.37883977C>G (hg19) ; chr17:g.39727724C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727724C>G , CM000679.2:g.39727724C>G	GRCh38
NC_000017.10:g.37883977C>G , CM000679.1:g.37883977C>G	GRCh37
NC_000017.9:g.35137503C>G	NCBI36
NG_007503.1:g.44585C>G , LRG_724:g.44585C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3448C>G MANE Select	ENSP00000269571.4:p.Pro1150Ala
ENST00000269571.9:c.3448C>G	ENSP00000269571.4:p.Pro1150Ala
ENST00000406381.6:c.3358C>G	ENSP00000385185.2:p.Pro1120Ala
ENST00000445658.6:c.2620C>G	ENSP00000404047.2:p.Pro874Ala
ENST00000541774.5:c.3403C>G	ENSP00000446466.1:p.Pro1135Ala
ENST00000578373.5:c.*3238C>G	ENSP00000463427.1:n.*3238C>G
ENST00000584450.5:c.*27C>G	ENSP00000463714.1:n.*27C>G
ENST00000584601.5:c.3358C>G	ENSP00000462438.1:p.Pro1120Ala
NM_001005862.2:c.3358C>G , LRG_724t1:c.3358C>G	NP_001005862.1:p.Pro1120Ala
NM_001289936.1:c.3403C>G , LRG_724t4:c.3403C>G	NP_001276865.1:p.Pro1135Ala
NM_001289937.1:c.*27C>G	NP_001276866.1:n.*27C>G
NM_004448.3:c.3448C>G , LRG_724t2:c.3448C>G	NP_004439.2:p.Pro1150Ala
NR_110535.1:n.3772C>G
XM_024450641.1:c.3586C>G	XP_024306409.1:p.Pro1196Ala
XM_024450642.1:c.3541C>G	XP_024306410.1:p.Pro1181Ala
XM_024450643.1:c.3496C>G	XP_024306411.1:p.Pro1166Ala
NM_001005862.3:c.3358C>G	NP_001005862.1:p.Pro1120Ala
NM_001289936.2:c.3403C>G	NP_001276865.1:p.Pro1135Ala
NM_001289937.2:c.*27C>G	NP_001276866.1:n.*27C>G
NM_001382782.1:c.3358C>G	NP_001369711.1:p.Pro1120Ala
NM_001382783.1:c.3358C>G	NP_001369712.1:p.Pro1120Ala
NM_001382784.1:c.3565C>G	NP_001369713.1:p.Pro1189Ala
NM_001382785.1:c.3550C>G	NP_001369714.1:p.Pro1184Ala
NM_001382786.1:c.3529C>G	NP_001369715.1:p.Pro1177Ala
NM_001382787.1:c.3523C>G	NP_001369716.1:p.Pro1175Ala
NM_001382788.1:c.3478C>G	NP_001369717.1:p.Pro1160Ala
NM_001382789.1:c.3469C>G	NP_001369718.1:p.Pro1157Ala
NM_001382790.1:c.3445C>G	NP_001369719.1:p.Pro1149Ala
NM_001382791.1:c.3439C>G	NP_001369720.1:p.Pro1147Ala
NM_001382792.1:c.3412C>G	NP_001369721.1:p.Pro1138Ala
NM_001382793.1:c.3406C>G	NP_001369722.1:p.Pro1136Ala
NM_001382794.1:c.3406C>G	NP_001369723.1:p.Pro1136Ala
NM_001382795.1:c.3400C>G	NP_001369724.1:p.Pro1134Ala
NM_001382796.1:c.3361C>G	NP_001369725.1:p.Pro1121Ala
NM_001382797.1:c.3349C>G	NP_001369726.1:p.Pro1117Ala
NM_001382798.1:c.3292C>G	NP_001369727.1:p.Pro1098Ala
NM_001382799.1:c.3268C>G	NP_001369728.1:p.Pro1090Ala
NM_001382800.1:c.3262C>G	NP_001369729.1:p.Pro1088Ala
NM_001382801.1:c.3244C>G	NP_001369730.1:p.Pro1082Ala
NM_001382802.1:c.3190C>G	NP_001369731.1:p.Pro1064Ala
NM_001382803.1:c.*27C>G	NP_001369732.1:n.*27C>G
NM_001382804.1:c.2620C>G	NP_001369733.1:p.Pro874Ala
NM_001382805.1:c.2497C>G	NP_001369734.1:p.Pro833Ala
NM_001382806.1:c.2410C>G	NP_001369735.1:p.Pro804Ala
NM_004448.4:c.3448C>G MANE Select	NP_004439.2:p.Pro1150Ala
NR_110535.2:n.3686C>G