Canonical Allele Identifier: CA399313424

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143299916
• MyVariant Identifiers: chr17:g.37884068T>G (hg19) ; chr17:g.39727815T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727815T>G , CM000679.2:g.39727815T>G	GRCh38
NC_000017.10:g.37884068T>G , CM000679.1:g.37884068T>G	GRCh37
NC_000017.9:g.35137594T>G	NCBI36
NG_007503.1:g.44676T>G , LRG_724:g.44676T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3539T>G MANE Select	ENSP00000269571.4:p.Val1180Gly
ENST00000269571.9:c.3539T>G	ENSP00000269571.4:p.Val1180Gly
ENST00000406381.6:c.3449T>G	ENSP00000385185.2:p.Val1150Gly
ENST00000445658.6:c.2711T>G	ENSP00000404047.2:p.Val904Gly
ENST00000541774.5:c.3494T>G	ENSP00000446466.1:p.Val1165Gly
ENST00000578373.5:c.*3329T>G	ENSP00000463427.1:n.*3329T>G
ENST00000584450.5:c.*118T>G	ENSP00000463714.1:n.*118T>G
ENST00000584601.5:c.3449T>G	ENSP00000462438.1:p.Val1150Gly
NM_001005862.2:c.3449T>G , LRG_724t1:c.3449T>G	NP_001005862.1:p.Val1150Gly
NM_001289936.1:c.3494T>G , LRG_724t4:c.3494T>G	NP_001276865.1:p.Val1165Gly
NM_001289937.1:c.*118T>G	NP_001276866.1:n.*118T>G
NM_004448.3:c.3539T>G , LRG_724t2:c.3539T>G	NP_004439.2:p.Val1180Gly
NR_110535.1:n.3863T>G
XM_024450641.1:c.3677T>G	XP_024306409.1:p.Val1226Gly
XM_024450642.1:c.3632T>G	XP_024306410.1:p.Val1211Gly
XM_024450643.1:c.3587T>G	XP_024306411.1:p.Val1196Gly
NM_001005862.3:c.3449T>G	NP_001005862.1:p.Val1150Gly
NM_001289936.2:c.3494T>G	NP_001276865.1:p.Val1165Gly
NM_001289937.2:c.*118T>G	NP_001276866.1:n.*118T>G
NM_001382782.1:c.3449T>G	NP_001369711.1:p.Val1150Gly
NM_001382783.1:c.3449T>G	NP_001369712.1:p.Val1150Gly
NM_001382784.1:c.3656T>G	NP_001369713.1:p.Val1219Gly
NM_001382785.1:c.3641T>G	NP_001369714.1:p.Val1214Gly
NM_001382786.1:c.3620T>G	NP_001369715.1:p.Val1207Gly
NM_001382787.1:c.3614T>G	NP_001369716.1:p.Val1205Gly
NM_001382788.1:c.3569T>G	NP_001369717.1:p.Val1190Gly
NM_001382789.1:c.3560T>G	NP_001369718.1:p.Val1187Gly
NM_001382790.1:c.3536T>G	NP_001369719.1:p.Val1179Gly
NM_001382791.1:c.3530T>G	NP_001369720.1:p.Val1177Gly
NM_001382792.1:c.3503T>G	NP_001369721.1:p.Val1168Gly
NM_001382793.1:c.3497T>G	NP_001369722.1:p.Val1166Gly
NM_001382794.1:c.3497T>G	NP_001369723.1:p.Val1166Gly
NM_001382795.1:c.3491T>G	NP_001369724.1:p.Val1164Gly
NM_001382796.1:c.3452T>G	NP_001369725.1:p.Val1151Gly
NM_001382797.1:c.3440T>G	NP_001369726.1:p.Val1147Gly
NM_001382798.1:c.3383T>G	NP_001369727.1:p.Val1128Gly
NM_001382799.1:c.3359T>G	NP_001369728.1:p.Val1120Gly
NM_001382800.1:c.3353T>G	NP_001369729.1:p.Val1118Gly
NM_001382801.1:c.3335T>G	NP_001369730.1:p.Val1112Gly
NM_001382802.1:c.3281T>G	NP_001369731.1:p.Val1094Gly
NM_001382803.1:c.*118T>G	NP_001369732.1:n.*118T>G
NM_001382804.1:c.2711T>G	NP_001369733.1:p.Val904Gly
NM_001382805.1:c.2588T>G	NP_001369734.1:p.Val863Gly
NM_001382806.1:c.2501T>G	NP_001369735.1:p.Val834Gly
NM_004448.4:c.3539T>G MANE Select	NP_004439.2:p.Val1180Gly
NR_110535.2:n.3777T>G