Canonical Allele Identifier: CA399312901

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3452C>A MANE Select	ENSP00000269571.4:p.Ser1151Ter
ENST00000269571.9:c.3452C>A	ENSP00000269571.4:p.Ser1151Ter
ENST00000406381.6:c.3362C>A	ENSP00000385185.2:p.Ser1121Ter
ENST00000445658.6:c.2624C>A	ENSP00000404047.2:p.Ser875Ter
ENST00000541774.5:c.3407C>A	ENSP00000446466.1:p.Ser1136Ter
ENST00000578373.5:c.*3242C>A	ENSP00000463427.1:n.*3242C>A
ENST00000584450.5:c.*31C>A	ENSP00000463714.1:n.*31C>A
ENST00000584601.5:c.3362C>A	ENSP00000462438.1:p.Ser1121Ter
NM_001005862.2:c.3362C>A , LRG_724t1:c.3362C>A	NP_001005862.1:p.Ser1121Ter
NM_001289936.1:c.3407C>A , LRG_724t4:c.3407C>A	NP_001276865.1:p.Ser1136Ter
NM_001289937.1:c.*31C>A	NP_001276866.1:n.*31C>A
NM_004448.3:c.3452C>A , LRG_724t2:c.3452C>A	NP_004439.2:p.Ser1151Ter
NR_110535.1:n.3776C>A
XM_024450641.1:c.3590C>A	XP_024306409.1:p.Ser1197Ter
XM_024450642.1:c.3545C>A	XP_024306410.1:p.Ser1182Ter
XM_024450643.1:c.3500C>A	XP_024306411.1:p.Ser1167Ter
NM_001005862.3:c.3362C>A	NP_001005862.1:p.Ser1121Ter
NM_001289936.2:c.3407C>A	NP_001276865.1:p.Ser1136Ter
NM_001289937.2:c.*31C>A	NP_001276866.1:n.*31C>A
NM_001382782.1:c.3362C>A	NP_001369711.1:p.Ser1121Ter
NM_001382783.1:c.3362C>A	NP_001369712.1:p.Ser1121Ter
NM_001382784.1:c.3569C>A	NP_001369713.1:p.Ser1190Ter
NM_001382785.1:c.3554C>A	NP_001369714.1:p.Ser1185Ter
NM_001382786.1:c.3533C>A	NP_001369715.1:p.Ser1178Ter
NM_001382787.1:c.3527C>A	NP_001369716.1:p.Ser1176Ter
NM_001382788.1:c.3482C>A	NP_001369717.1:p.Ser1161Ter
NM_001382789.1:c.3473C>A	NP_001369718.1:p.Ser1158Ter
NM_001382790.1:c.3449C>A	NP_001369719.1:p.Ser1150Ter
NM_001382791.1:c.3443C>A	NP_001369720.1:p.Ser1148Ter
NM_001382792.1:c.3416C>A	NP_001369721.1:p.Ser1139Ter
NM_001382793.1:c.3410C>A	NP_001369722.1:p.Ser1137Ter
NM_001382794.1:c.3410C>A	NP_001369723.1:p.Ser1137Ter
NM_001382795.1:c.3404C>A	NP_001369724.1:p.Ser1135Ter
NM_001382796.1:c.3365C>A	NP_001369725.1:p.Ser1122Ter
NM_001382797.1:c.3353C>A	NP_001369726.1:p.Ser1118Ter
NM_001382798.1:c.3296C>A	NP_001369727.1:p.Ser1099Ter
NM_001382799.1:c.3272C>A	NP_001369728.1:p.Ser1091Ter
NM_001382800.1:c.3266C>A	NP_001369729.1:p.Ser1089Ter
NM_001382801.1:c.3248C>A	NP_001369730.1:p.Ser1083Ter
NM_001382802.1:c.3194C>A	NP_001369731.1:p.Ser1065Ter
NM_001382803.1:c.*31C>A	NP_001369732.1:n.*31C>A
NM_001382804.1:c.2624C>A	NP_001369733.1:p.Ser875Ter
NM_001382805.1:c.2501C>A	NP_001369734.1:p.Ser834Ter
NM_001382806.1:c.2414C>A	NP_001369735.1:p.Ser805Ter
NM_004448.4:c.3452C>A MANE Select	NP_004439.2:p.Ser1151Ter
NR_110535.2:n.3690C>A