Canonical Allele Identifier: CA499670866

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145849007
• MyVariant Identifiers: chr17:g.37881029G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724776G>C , CM000679.2:g.39724776G>C	GRCh38
NC_000017.10:g.37881029G>C , CM000679.1:g.37881029G>C	GRCh37
NC_000017.9:g.35134555G>C	NCBI36
NG_007503.1:g.41637G>C , LRG_724:g.41637G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2358G>C MANE Select	ENSP00000269571.4:p.Leu786=
ENST00000269571.9:c.2358G>C	ENSP00000269571.4:p.Leu786=
ENST00000406381.6:c.2268G>C	ENSP00000385185.2:p.Leu756=
ENST00000445658.6:c.1530G>C	ENSP00000404047.2:p.Leu510=
ENST00000541774.5:c.2313G>C	ENSP00000446466.1:p.Leu771=
ENST00000578373.5:c.*2148G>C	ENSP00000463427.1:n.*2148G>C
ENST00000580074.1:c.464G>C
ENST00000583038.5:n.3492G>C
ENST00000584450.5:c.2358G>C	ENSP00000463714.1:p.Leu786=
ENST00000584601.5:c.2268G>C	ENSP00000462438.1:p.Leu756=
NM_001005862.2:c.2268G>C , LRG_724t1:c.2268G>C	NP_001005862.1:p.Leu756=
NM_001289936.1:c.2313G>C , LRG_724t4:c.2313G>C	NP_001276865.1:p.Leu771=
NM_001289937.1:c.2358G>C	NP_001276866.1:p.Leu786=
NM_004448.3:c.2358G>C , LRG_724t2:c.2358G>C	NP_004439.2:p.Leu786=
NR_110535.1:n.2682G>C
XM_024450641.1:c.2496G>C	XP_024306409.1:p.Leu832=
XM_024450642.1:c.2451G>C	XP_024306410.1:p.Leu817=
XM_024450643.1:c.2406G>C	XP_024306411.1:p.Leu802=
NM_001005862.3:c.2268G>C	NP_001005862.1:p.Leu756=
NM_001289936.2:c.2313G>C	NP_001276865.1:p.Leu771=
NM_001289937.2:c.2358G>C	NP_001276866.1:p.Leu786=
NM_001382782.1:c.2268G>C	NP_001369711.1:p.Leu756=
NM_001382783.1:c.2268G>C	NP_001369712.1:p.Leu756=
NM_001382784.1:c.2475G>C	NP_001369713.1:p.Leu825=
NM_001382785.1:c.2460G>C	NP_001369714.1:p.Leu820=
NM_001382786.1:c.2439G>C	NP_001369715.1:p.Leu813=
NM_001382787.1:c.2433G>C	NP_001369716.1:p.Leu811=
NM_001382788.1:c.2388G>C	NP_001369717.1:p.Leu796=
NM_001382789.1:c.2379G>C	NP_001369718.1:p.Leu793=
NM_001382790.1:c.2355G>C	NP_001369719.1:p.Leu785=
NM_001382791.1:c.2349G>C	NP_001369720.1:p.Leu783=
NM_001382792.1:c.2322G>C	NP_001369721.1:p.Leu774=
NM_001382793.1:c.2316G>C	NP_001369722.1:p.Leu772=
NM_001382794.1:c.2316G>C	NP_001369723.1:p.Leu772=
NM_001382795.1:c.2310G>C	NP_001369724.1:p.Leu770=
NM_001382796.1:c.2358G>C	NP_001369725.1:p.Leu786=
NM_001382797.1:c.2259G>C	NP_001369726.1:p.Leu753=
NM_001382798.1:c.2358G>C	NP_001369727.1:p.Leu786=
NM_001382799.1:c.2178G>C	NP_001369728.1:p.Leu726=
NM_001382800.1:c.2308-273G>C	NP_001369729.1:n.2308-273G>C
NM_001382801.1:c.2310G>C	NP_001369730.1:p.Leu770=
NM_001382802.1:c.2100G>C	NP_001369731.1:p.Leu700=
NM_001382803.1:c.2316G>C	NP_001369732.1:p.Leu772=
NM_001382804.1:c.1530G>C	NP_001369733.1:p.Leu510=
NM_001382805.1:c.2208+1116G>C	NP_001369734.1:n.2208+1116G>C
NM_001382806.1:c.1320G>C	NP_001369735.1:p.Leu440=
NM_004448.4:c.2358G>C MANE Select	NP_004439.2:p.Leu786=
NR_110535.2:n.2596G>C