Canonical Allele Identifier: CA399312902

Gene: ERBB2

Linked Data

• dbSNP Id: rs1357550606
• MyVariant Identifiers: chr17:g.37883981C>G (hg19) ; chr17:g.39727728C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727728C>G , CM000679.2:g.39727728C>G	GRCh38
NC_000017.10:g.37883981C>G , CM000679.1:g.37883981C>G	GRCh37
NC_000017.9:g.35137507C>G	NCBI36
NG_007503.1:g.44589C>G , LRG_724:g.44589C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3452C>G MANE Select	ENSP00000269571.4:p.Ser1151Trp
ENST00000269571.9:c.3452C>G	ENSP00000269571.4:p.Ser1151Trp
ENST00000406381.6:c.3362C>G	ENSP00000385185.2:p.Ser1121Trp
ENST00000445658.6:c.2624C>G	ENSP00000404047.2:p.Ser875Trp
ENST00000541774.5:c.3407C>G	ENSP00000446466.1:p.Ser1136Trp
ENST00000578373.5:c.*3242C>G	ENSP00000463427.1:n.*3242C>G
ENST00000584450.5:c.*31C>G	ENSP00000463714.1:n.*31C>G
ENST00000584601.5:c.3362C>G	ENSP00000462438.1:p.Ser1121Trp
NM_001005862.2:c.3362C>G , LRG_724t1:c.3362C>G	NP_001005862.1:p.Ser1121Trp
NM_001289936.1:c.3407C>G , LRG_724t4:c.3407C>G	NP_001276865.1:p.Ser1136Trp
NM_001289937.1:c.*31C>G	NP_001276866.1:n.*31C>G
NM_004448.3:c.3452C>G , LRG_724t2:c.3452C>G	NP_004439.2:p.Ser1151Trp
NR_110535.1:n.3776C>G
XM_024450641.1:c.3590C>G	XP_024306409.1:p.Ser1197Trp
XM_024450642.1:c.3545C>G	XP_024306410.1:p.Ser1182Trp
XM_024450643.1:c.3500C>G	XP_024306411.1:p.Ser1167Trp
NM_001005862.3:c.3362C>G	NP_001005862.1:p.Ser1121Trp
NM_001289936.2:c.3407C>G	NP_001276865.1:p.Ser1136Trp
NM_001289937.2:c.*31C>G	NP_001276866.1:n.*31C>G
NM_001382782.1:c.3362C>G	NP_001369711.1:p.Ser1121Trp
NM_001382783.1:c.3362C>G	NP_001369712.1:p.Ser1121Trp
NM_001382784.1:c.3569C>G	NP_001369713.1:p.Ser1190Trp
NM_001382785.1:c.3554C>G	NP_001369714.1:p.Ser1185Trp
NM_001382786.1:c.3533C>G	NP_001369715.1:p.Ser1178Trp
NM_001382787.1:c.3527C>G	NP_001369716.1:p.Ser1176Trp
NM_001382788.1:c.3482C>G	NP_001369717.1:p.Ser1161Trp
NM_001382789.1:c.3473C>G	NP_001369718.1:p.Ser1158Trp
NM_001382790.1:c.3449C>G	NP_001369719.1:p.Ser1150Trp
NM_001382791.1:c.3443C>G	NP_001369720.1:p.Ser1148Trp
NM_001382792.1:c.3416C>G	NP_001369721.1:p.Ser1139Trp
NM_001382793.1:c.3410C>G	NP_001369722.1:p.Ser1137Trp
NM_001382794.1:c.3410C>G	NP_001369723.1:p.Ser1137Trp
NM_001382795.1:c.3404C>G	NP_001369724.1:p.Ser1135Trp
NM_001382796.1:c.3365C>G	NP_001369725.1:p.Ser1122Trp
NM_001382797.1:c.3353C>G	NP_001369726.1:p.Ser1118Trp
NM_001382798.1:c.3296C>G	NP_001369727.1:p.Ser1099Trp
NM_001382799.1:c.3272C>G	NP_001369728.1:p.Ser1091Trp
NM_001382800.1:c.3266C>G	NP_001369729.1:p.Ser1089Trp
NM_001382801.1:c.3248C>G	NP_001369730.1:p.Ser1083Trp
NM_001382802.1:c.3194C>G	NP_001369731.1:p.Ser1065Trp
NM_001382803.1:c.*31C>G	NP_001369732.1:n.*31C>G
NM_001382804.1:c.2624C>G	NP_001369733.1:p.Ser875Trp
NM_001382805.1:c.2501C>G	NP_001369734.1:p.Ser834Trp
NM_001382806.1:c.2414C>G	NP_001369735.1:p.Ser805Trp
NM_004448.4:c.3452C>G MANE Select	NP_004439.2:p.Ser1151Trp
NR_110535.2:n.3690C>G