Canonical Allele Identifier: CA399303070

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2367C>G MANE Select	ENSP00000269571.4:p.Cys789Trp
ENST00000269571.9:c.2367C>G	ENSP00000269571.4:p.Cys789Trp
ENST00000406381.6:c.2277C>G	ENSP00000385185.2:p.Cys759Trp
ENST00000445658.6:c.1539C>G	ENSP00000404047.2:p.Cys513Trp
ENST00000541774.5:c.2322C>G	ENSP00000446466.1:p.Cys774Trp
ENST00000578373.5:c.*2157C>G	ENSP00000463427.1:n.*2157C>G
ENST00000580074.1:c.473C>G
ENST00000583038.5:n.3501C>G
ENST00000584450.5:c.2367C>G	ENSP00000463714.1:p.Cys789Trp
ENST00000584601.5:c.2277C>G	ENSP00000462438.1:p.Cys759Trp
NM_001005862.2:c.2277C>G , LRG_724t1:c.2277C>G	NP_001005862.1:p.Cys759Trp
NM_001289936.1:c.2322C>G , LRG_724t4:c.2322C>G	NP_001276865.1:p.Cys774Trp
NM_001289937.1:c.2367C>G	NP_001276866.1:p.Cys789Trp
NM_004448.3:c.2367C>G , LRG_724t2:c.2367C>G	NP_004439.2:p.Cys789Trp
NR_110535.1:n.2691C>G
XM_024450641.1:c.2505C>G	XP_024306409.1:p.Cys835Trp
XM_024450642.1:c.2460C>G	XP_024306410.1:p.Cys820Trp
XM_024450643.1:c.2415C>G	XP_024306411.1:p.Cys805Trp
NM_001005862.3:c.2277C>G	NP_001005862.1:p.Cys759Trp
NM_001289936.2:c.2322C>G	NP_001276865.1:p.Cys774Trp
NM_001289937.2:c.2367C>G	NP_001276866.1:p.Cys789Trp
NM_001382782.1:c.2277C>G	NP_001369711.1:p.Cys759Trp
NM_001382783.1:c.2277C>G	NP_001369712.1:p.Cys759Trp
NM_001382784.1:c.2484C>G	NP_001369713.1:p.Cys828Trp
NM_001382785.1:c.2469C>G	NP_001369714.1:p.Cys823Trp
NM_001382786.1:c.2448C>G	NP_001369715.1:p.Cys816Trp
NM_001382787.1:c.2442C>G	NP_001369716.1:p.Cys814Trp
NM_001382788.1:c.2397C>G	NP_001369717.1:p.Cys799Trp
NM_001382789.1:c.2388C>G	NP_001369718.1:p.Cys796Trp
NM_001382790.1:c.2364C>G	NP_001369719.1:p.Cys788Trp
NM_001382791.1:c.2358C>G	NP_001369720.1:p.Cys786Trp
NM_001382792.1:c.2331C>G	NP_001369721.1:p.Cys777Trp
NM_001382793.1:c.2325C>G	NP_001369722.1:p.Cys775Trp
NM_001382794.1:c.2325C>G	NP_001369723.1:p.Cys775Trp
NM_001382795.1:c.2319C>G	NP_001369724.1:p.Cys773Trp
NM_001382796.1:c.2367C>G	NP_001369725.1:p.Cys789Trp
NM_001382797.1:c.2268C>G	NP_001369726.1:p.Cys756Trp
NM_001382798.1:c.2367C>G	NP_001369727.1:p.Cys789Trp
NM_001382799.1:c.2187C>G	NP_001369728.1:p.Cys729Trp
NM_001382800.1:c.2308-264C>G	NP_001369729.1:n.2308-264C>G
NM_001382801.1:c.2319C>G	NP_001369730.1:p.Cys773Trp
NM_001382802.1:c.2109C>G	NP_001369731.1:p.Cys703Trp
NM_001382803.1:c.2325C>G	NP_001369732.1:p.Cys775Trp
NM_001382804.1:c.1539C>G	NP_001369733.1:p.Cys513Trp
NM_001382805.1:c.2208+1125C>G	NP_001369734.1:n.2208+1125C>G
NM_001382806.1:c.1329C>G	NP_001369735.1:p.Cys443Trp
NM_004448.4:c.2367C>G MANE Select	NP_004439.2:p.Cys789Trp
NR_110535.2:n.2605C>G