Canonical Allele Identifier: CA399303068

Gene: ERBB2

Linked Data

• dbSNP Id: rs1164926091
• MyVariant Identifiers: chr17:g.37881038C>A (hg19) ; chr17:g.39724785C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724785C>A , CM000679.2:g.39724785C>A	GRCh38
NC_000017.10:g.37881038C>A , CM000679.1:g.37881038C>A	GRCh37
NC_000017.9:g.35134564C>A	NCBI36
NG_007503.1:g.41646C>A , LRG_724:g.41646C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2367C>A MANE Select	ENSP00000269571.4:p.Cys789Ter
ENST00000269571.9:c.2367C>A	ENSP00000269571.4:p.Cys789Ter
ENST00000406381.6:c.2277C>A	ENSP00000385185.2:p.Cys759Ter
ENST00000445658.6:c.1539C>A	ENSP00000404047.2:p.Cys513Ter
ENST00000541774.5:c.2322C>A	ENSP00000446466.1:p.Cys774Ter
ENST00000578373.5:c.*2157C>A	ENSP00000463427.1:n.*2157C>A
ENST00000580074.1:c.473C>A
ENST00000583038.5:n.3501C>A
ENST00000584450.5:c.2367C>A	ENSP00000463714.1:p.Cys789Ter
ENST00000584601.5:c.2277C>A	ENSP00000462438.1:p.Cys759Ter
NM_001005862.2:c.2277C>A , LRG_724t1:c.2277C>A	NP_001005862.1:p.Cys759Ter
NM_001289936.1:c.2322C>A , LRG_724t4:c.2322C>A	NP_001276865.1:p.Cys774Ter
NM_001289937.1:c.2367C>A	NP_001276866.1:p.Cys789Ter
NM_004448.3:c.2367C>A , LRG_724t2:c.2367C>A	NP_004439.2:p.Cys789Ter
NR_110535.1:n.2691C>A
XM_024450641.1:c.2505C>A	XP_024306409.1:p.Cys835Ter
XM_024450642.1:c.2460C>A	XP_024306410.1:p.Cys820Ter
XM_024450643.1:c.2415C>A	XP_024306411.1:p.Cys805Ter
NM_001005862.3:c.2277C>A	NP_001005862.1:p.Cys759Ter
NM_001289936.2:c.2322C>A	NP_001276865.1:p.Cys774Ter
NM_001289937.2:c.2367C>A	NP_001276866.1:p.Cys789Ter
NM_001382782.1:c.2277C>A	NP_001369711.1:p.Cys759Ter
NM_001382783.1:c.2277C>A	NP_001369712.1:p.Cys759Ter
NM_001382784.1:c.2484C>A	NP_001369713.1:p.Cys828Ter
NM_001382785.1:c.2469C>A	NP_001369714.1:p.Cys823Ter
NM_001382786.1:c.2448C>A	NP_001369715.1:p.Cys816Ter
NM_001382787.1:c.2442C>A	NP_001369716.1:p.Cys814Ter
NM_001382788.1:c.2397C>A	NP_001369717.1:p.Cys799Ter
NM_001382789.1:c.2388C>A	NP_001369718.1:p.Cys796Ter
NM_001382790.1:c.2364C>A	NP_001369719.1:p.Cys788Ter
NM_001382791.1:c.2358C>A	NP_001369720.1:p.Cys786Ter
NM_001382792.1:c.2331C>A	NP_001369721.1:p.Cys777Ter
NM_001382793.1:c.2325C>A	NP_001369722.1:p.Cys775Ter
NM_001382794.1:c.2325C>A	NP_001369723.1:p.Cys775Ter
NM_001382795.1:c.2319C>A	NP_001369724.1:p.Cys773Ter
NM_001382796.1:c.2367C>A	NP_001369725.1:p.Cys789Ter
NM_001382797.1:c.2268C>A	NP_001369726.1:p.Cys756Ter
NM_001382798.1:c.2367C>A	NP_001369727.1:p.Cys789Ter
NM_001382799.1:c.2187C>A	NP_001369728.1:p.Cys729Ter
NM_001382800.1:c.2308-264C>A	NP_001369729.1:n.2308-264C>A
NM_001382801.1:c.2319C>A	NP_001369730.1:p.Cys773Ter
NM_001382802.1:c.2109C>A	NP_001369731.1:p.Cys703Ter
NM_001382803.1:c.2325C>A	NP_001369732.1:p.Cys775Ter
NM_001382804.1:c.1539C>A	NP_001369733.1:p.Cys513Ter
NM_001382805.1:c.2208+1125C>A	NP_001369734.1:n.2208+1125C>A
NM_001382806.1:c.1329C>A	NP_001369735.1:p.Cys443Ter
NM_004448.4:c.2367C>A MANE Select	NP_004439.2:p.Cys789Ter
NR_110535.2:n.2605C>A