Canonical Allele Identifier: CA399313025

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143293146
• MyVariant Identifiers: chr17:g.37884008C>G (hg19) ; chr17:g.39727755C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727755C>G , CM000679.2:g.39727755C>G	GRCh38
NC_000017.10:g.37884008C>G , CM000679.1:g.37884008C>G	GRCh37
NC_000017.9:g.35137534C>G	NCBI36
NG_007503.1:g.44616C>G , LRG_724:g.44616C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3479C>G MANE Select	ENSP00000269571.4:p.Ala1160Gly
ENST00000269571.9:c.3479C>G	ENSP00000269571.4:p.Ala1160Gly
ENST00000406381.6:c.3389C>G	ENSP00000385185.2:p.Ala1130Gly
ENST00000445658.6:c.2651C>G	ENSP00000404047.2:p.Ala884Gly
ENST00000541774.5:c.3434C>G	ENSP00000446466.1:p.Ala1145Gly
ENST00000578373.5:c.*3269C>G	ENSP00000463427.1:n.*3269C>G
ENST00000584450.5:c.*58C>G	ENSP00000463714.1:n.*58C>G
ENST00000584601.5:c.3389C>G	ENSP00000462438.1:p.Ala1130Gly
NM_001005862.2:c.3389C>G , LRG_724t1:c.3389C>G	NP_001005862.1:p.Ala1130Gly
NM_001289936.1:c.3434C>G , LRG_724t4:c.3434C>G	NP_001276865.1:p.Ala1145Gly
NM_001289937.1:c.*58C>G	NP_001276866.1:n.*58C>G
NM_004448.3:c.3479C>G , LRG_724t2:c.3479C>G	NP_004439.2:p.Ala1160Gly
NR_110535.1:n.3803C>G
XM_024450641.1:c.3617C>G	XP_024306409.1:p.Ala1206Gly
XM_024450642.1:c.3572C>G	XP_024306410.1:p.Ala1191Gly
XM_024450643.1:c.3527C>G	XP_024306411.1:p.Ala1176Gly
NM_001005862.3:c.3389C>G	NP_001005862.1:p.Ala1130Gly
NM_001289936.2:c.3434C>G	NP_001276865.1:p.Ala1145Gly
NM_001289937.2:c.*58C>G	NP_001276866.1:n.*58C>G
NM_001382782.1:c.3389C>G	NP_001369711.1:p.Ala1130Gly
NM_001382783.1:c.3389C>G	NP_001369712.1:p.Ala1130Gly
NM_001382784.1:c.3596C>G	NP_001369713.1:p.Ala1199Gly
NM_001382785.1:c.3581C>G	NP_001369714.1:p.Ala1194Gly
NM_001382786.1:c.3560C>G	NP_001369715.1:p.Ala1187Gly
NM_001382787.1:c.3554C>G	NP_001369716.1:p.Ala1185Gly
NM_001382788.1:c.3509C>G	NP_001369717.1:p.Ala1170Gly
NM_001382789.1:c.3500C>G	NP_001369718.1:p.Ala1167Gly
NM_001382790.1:c.3476C>G	NP_001369719.1:p.Ala1159Gly
NM_001382791.1:c.3470C>G	NP_001369720.1:p.Ala1157Gly
NM_001382792.1:c.3443C>G	NP_001369721.1:p.Ala1148Gly
NM_001382793.1:c.3437C>G	NP_001369722.1:p.Ala1146Gly
NM_001382794.1:c.3437C>G	NP_001369723.1:p.Ala1146Gly
NM_001382795.1:c.3431C>G	NP_001369724.1:p.Ala1144Gly
NM_001382796.1:c.3392C>G	NP_001369725.1:p.Ala1131Gly
NM_001382797.1:c.3380C>G	NP_001369726.1:p.Ala1127Gly
NM_001382798.1:c.3323C>G	NP_001369727.1:p.Ala1108Gly
NM_001382799.1:c.3299C>G	NP_001369728.1:p.Ala1100Gly
NM_001382800.1:c.3293C>G	NP_001369729.1:p.Ala1098Gly
NM_001382801.1:c.3275C>G	NP_001369730.1:p.Ala1092Gly
NM_001382802.1:c.3221C>G	NP_001369731.1:p.Ala1074Gly
NM_001382803.1:c.*58C>G	NP_001369732.1:n.*58C>G
NM_001382804.1:c.2651C>G	NP_001369733.1:p.Ala884Gly
NM_001382805.1:c.2528C>G	NP_001369734.1:p.Ala843Gly
NM_001382806.1:c.2441C>G	NP_001369735.1:p.Ala814Gly
NM_004448.4:c.3479C>G MANE Select	NP_004439.2:p.Ala1160Gly
NR_110535.2:n.3717C>G