Canonical Allele Identifier: CA399312664

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143254884
• MyVariant Identifiers: chr17:g.37883749C>G (hg19) ; chr17:g.39727496C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727496C>G , CM000679.2:g.39727496C>G	GRCh38
NC_000017.10:g.37883749C>G , CM000679.1:g.37883749C>G	GRCh37
NC_000017.9:g.35137275C>G	NCBI36
NG_007503.1:g.44357C>G , LRG_724:g.44357C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3361C>G MANE Select	ENSP00000269571.4:p.Pro1121Ala
ENST00000269571.9:c.3361C>G	ENSP00000269571.4:p.Pro1121Ala
ENST00000406381.6:c.3271C>G	ENSP00000385185.2:p.Pro1091Ala
ENST00000445658.6:c.2533C>G	ENSP00000404047.2:p.Pro845Ala
ENST00000541774.5:c.3316C>G	ENSP00000446466.1:p.Pro1106Ala
ENST00000578373.5:c.*3151C>G	ENSP00000463427.1:n.*3151C>G
ENST00000584450.5:c.3160-193C>G	ENSP00000463714.1:n.3160-193C>G
ENST00000584601.5:c.3271C>G	ENSP00000462438.1:p.Pro1091Ala
NM_001005862.2:c.3271C>G , LRG_724t1:c.3271C>G	NP_001005862.1:p.Pro1091Ala
NM_001289936.1:c.3316C>G , LRG_724t4:c.3316C>G	NP_001276865.1:p.Pro1106Ala
NM_001289937.1:c.3160-193C>G	NP_001276866.1:n.3160-193C>G
NM_004448.3:c.3361C>G , LRG_724t2:c.3361C>G	NP_004439.2:p.Pro1121Ala
NR_110535.1:n.3685C>G
XM_024450641.1:c.3499C>G	XP_024306409.1:p.Pro1167Ala
XM_024450642.1:c.3454C>G	XP_024306410.1:p.Pro1152Ala
XM_024450643.1:c.3409C>G	XP_024306411.1:p.Pro1137Ala
NM_001005862.3:c.3271C>G	NP_001005862.1:p.Pro1091Ala
NM_001289936.2:c.3316C>G	NP_001276865.1:p.Pro1106Ala
NM_001289937.2:c.3160-193C>G	NP_001276866.1:n.3160-193C>G
NM_001382782.1:c.3271C>G	NP_001369711.1:p.Pro1091Ala
NM_001382783.1:c.3271C>G	NP_001369712.1:p.Pro1091Ala
NM_001382784.1:c.3478C>G	NP_001369713.1:p.Pro1160Ala
NM_001382785.1:c.3463C>G	NP_001369714.1:p.Pro1155Ala
NM_001382786.1:c.3442C>G	NP_001369715.1:p.Pro1148Ala
NM_001382787.1:c.3436C>G	NP_001369716.1:p.Pro1146Ala
NM_001382788.1:c.3391C>G	NP_001369717.1:p.Pro1131Ala
NM_001382789.1:c.3382C>G	NP_001369718.1:p.Pro1128Ala
NM_001382790.1:c.3358C>G	NP_001369719.1:p.Pro1120Ala
NM_001382791.1:c.3352C>G	NP_001369720.1:p.Pro1118Ala
NM_001382792.1:c.3325C>G	NP_001369721.1:p.Pro1109Ala
NM_001382793.1:c.3319C>G	NP_001369722.1:p.Pro1107Ala
NM_001382794.1:c.3319C>G	NP_001369723.1:p.Pro1107Ala
NM_001382795.1:c.3313C>G	NP_001369724.1:p.Pro1105Ala
NM_001382796.1:c.3274C>G	NP_001369725.1:p.Pro1092Ala
NM_001382797.1:c.3262C>G	NP_001369726.1:p.Pro1088Ala
NM_001382798.1:c.3205C>G	NP_001369727.1:p.Pro1069Ala
NM_001382799.1:c.3181C>G	NP_001369728.1:p.Pro1061Ala
NM_001382800.1:c.3175C>G	NP_001369729.1:p.Pro1059Ala
NM_001382801.1:c.3157C>G	NP_001369730.1:p.Pro1053Ala
NM_001382802.1:c.3103C>G	NP_001369731.1:p.Pro1035Ala
NM_001382803.1:c.3118-193C>G	NP_001369732.1:n.3118-193C>G
NM_001382804.1:c.2533C>G	NP_001369733.1:p.Pro845Ala
NM_001382805.1:c.2410C>G	NP_001369734.1:p.Pro804Ala
NM_001382806.1:c.2323C>G	NP_001369735.1:p.Pro775Ala
NM_004448.4:c.3361C>G MANE Select	NP_004439.2:p.Pro1121Ala
NR_110535.2:n.3599C>G