Canonical Allele Identifier: CA399310388

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143239064
• MyVariant Identifiers: chr17:g.37883615C>G (hg19) ; chr17:g.39727362C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727362C>G , CM000679.2:g.39727362C>G	GRCh38
NC_000017.10:g.37883615C>G , CM000679.1:g.37883615C>G	GRCh37
NC_000017.9:g.35137141C>G	NCBI36
NG_007503.1:g.44223C>G , LRG_724:g.44223C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3227C>G MANE Select	ENSP00000269571.4:p.Ala1076Gly
ENST00000269571.9:c.3227C>G	ENSP00000269571.4:p.Ala1076Gly
ENST00000406381.6:c.3137C>G	ENSP00000385185.2:p.Ala1046Gly
ENST00000445658.6:c.2399C>G	ENSP00000404047.2:p.Ala800Gly
ENST00000541774.5:c.3182C>G	ENSP00000446466.1:p.Ala1061Gly
ENST00000578373.5:c.*3017C>G	ENSP00000463427.1:n.*3017C>G
ENST00000584450.5:c.3160-327C>G	ENSP00000463714.1:n.3160-327C>G
ENST00000584601.5:c.3137C>G	ENSP00000462438.1:p.Ala1046Gly
NM_001005862.2:c.3137C>G , LRG_724t1:c.3137C>G	NP_001005862.1:p.Ala1046Gly
NM_001289936.1:c.3182C>G , LRG_724t4:c.3182C>G	NP_001276865.1:p.Ala1061Gly
NM_001289937.1:c.3160-327C>G	NP_001276866.1:n.3160-327C>G
NM_004448.3:c.3227C>G , LRG_724t2:c.3227C>G	NP_004439.2:p.Ala1076Gly
NR_110535.1:n.3551C>G
XM_024450641.1:c.3365C>G	XP_024306409.1:p.Ala1122Gly
XM_024450642.1:c.3320C>G	XP_024306410.1:p.Ala1107Gly
XM_024450643.1:c.3275C>G	XP_024306411.1:p.Ala1092Gly
NM_001005862.3:c.3137C>G	NP_001005862.1:p.Ala1046Gly
NM_001289936.2:c.3182C>G	NP_001276865.1:p.Ala1061Gly
NM_001289937.2:c.3160-327C>G	NP_001276866.1:n.3160-327C>G
NM_001382782.1:c.3137C>G	NP_001369711.1:p.Ala1046Gly
NM_001382783.1:c.3137C>G	NP_001369712.1:p.Ala1046Gly
NM_001382784.1:c.3344C>G	NP_001369713.1:p.Ala1115Gly
NM_001382785.1:c.3329C>G	NP_001369714.1:p.Ala1110Gly
NM_001382786.1:c.3308C>G	NP_001369715.1:p.Ala1103Gly
NM_001382787.1:c.3302C>G	NP_001369716.1:p.Ala1101Gly
NM_001382788.1:c.3257C>G	NP_001369717.1:p.Ala1086Gly
NM_001382789.1:c.3248C>G	NP_001369718.1:p.Ala1083Gly
NM_001382790.1:c.3224C>G	NP_001369719.1:p.Ala1075Gly
NM_001382791.1:c.3218C>G	NP_001369720.1:p.Ala1073Gly
NM_001382792.1:c.3191C>G	NP_001369721.1:p.Ala1064Gly
NM_001382793.1:c.3185C>G	NP_001369722.1:p.Ala1062Gly
NM_001382794.1:c.3185C>G	NP_001369723.1:p.Ala1062Gly
NM_001382795.1:c.3179C>G	NP_001369724.1:p.Ala1060Gly
NM_001382796.1:c.3140C>G	NP_001369725.1:p.Ala1047Gly
NM_001382797.1:c.3128C>G	NP_001369726.1:p.Ala1043Gly
NM_001382798.1:c.3071C>G	NP_001369727.1:p.Ala1024Gly
NM_001382799.1:c.3047C>G	NP_001369728.1:p.Ala1016Gly
NM_001382800.1:c.3041C>G	NP_001369729.1:p.Ala1014Gly
NM_001382801.1:c.3023C>G	NP_001369730.1:p.Ala1008Gly
NM_001382802.1:c.2969C>G	NP_001369731.1:p.Ala990Gly
NM_001382803.1:c.3118-327C>G	NP_001369732.1:n.3118-327C>G
NM_001382804.1:c.2399C>G	NP_001369733.1:p.Ala800Gly
NM_001382805.1:c.2276C>G	NP_001369734.1:p.Ala759Gly
NM_001382806.1:c.2189C>G	NP_001369735.1:p.Ala730Gly
NM_004448.4:c.3227C>G MANE Select	NP_004439.2:p.Ala1076Gly
NR_110535.2:n.3465C>G