Canonical Allele Identifier: CA399303005

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145849087
• MyVariant Identifiers: chr17:g.37881030G>C (hg19) ; chr17:g.39724777G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724777G>C , CM000679.2:g.39724777G>C	GRCh38
NC_000017.10:g.37881030G>C , CM000679.1:g.37881030G>C	GRCh37
NC_000017.9:g.35134556G>C	NCBI36
NG_007503.1:g.41638G>C , LRG_724:g.41638G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2359G>C MANE Select	ENSP00000269571.4:p.Gly787Arg
ENST00000269571.9:c.2359G>C	ENSP00000269571.4:p.Gly787Arg
ENST00000406381.6:c.2269G>C	ENSP00000385185.2:p.Gly757Arg
ENST00000445658.6:c.1531G>C	ENSP00000404047.2:p.Gly511Arg
ENST00000541774.5:c.2314G>C	ENSP00000446466.1:p.Gly772Arg
ENST00000578373.5:c.*2149G>C	ENSP00000463427.1:n.*2149G>C
ENST00000580074.1:c.465G>C
ENST00000583038.5:n.3493G>C
ENST00000584450.5:c.2359G>C	ENSP00000463714.1:p.Gly787Arg
ENST00000584601.5:c.2269G>C	ENSP00000462438.1:p.Gly757Arg
NM_001005862.2:c.2269G>C , LRG_724t1:c.2269G>C	NP_001005862.1:p.Gly757Arg
NM_001289936.1:c.2314G>C , LRG_724t4:c.2314G>C	NP_001276865.1:p.Gly772Arg
NM_001289937.1:c.2359G>C	NP_001276866.1:p.Gly787Arg
NM_004448.3:c.2359G>C , LRG_724t2:c.2359G>C	NP_004439.2:p.Gly787Arg
NR_110535.1:n.2683G>C
XM_024450641.1:c.2497G>C	XP_024306409.1:p.Gly833Arg
XM_024450642.1:c.2452G>C	XP_024306410.1:p.Gly818Arg
XM_024450643.1:c.2407G>C	XP_024306411.1:p.Gly803Arg
NM_001005862.3:c.2269G>C	NP_001005862.1:p.Gly757Arg
NM_001289936.2:c.2314G>C	NP_001276865.1:p.Gly772Arg
NM_001289937.2:c.2359G>C	NP_001276866.1:p.Gly787Arg
NM_001382782.1:c.2269G>C	NP_001369711.1:p.Gly757Arg
NM_001382783.1:c.2269G>C	NP_001369712.1:p.Gly757Arg
NM_001382784.1:c.2476G>C	NP_001369713.1:p.Gly826Arg
NM_001382785.1:c.2461G>C	NP_001369714.1:p.Gly821Arg
NM_001382786.1:c.2440G>C	NP_001369715.1:p.Gly814Arg
NM_001382787.1:c.2434G>C	NP_001369716.1:p.Gly812Arg
NM_001382788.1:c.2389G>C	NP_001369717.1:p.Gly797Arg
NM_001382789.1:c.2380G>C	NP_001369718.1:p.Gly794Arg
NM_001382790.1:c.2356G>C	NP_001369719.1:p.Gly786Arg
NM_001382791.1:c.2350G>C	NP_001369720.1:p.Gly784Arg
NM_001382792.1:c.2323G>C	NP_001369721.1:p.Gly775Arg
NM_001382793.1:c.2317G>C	NP_001369722.1:p.Gly773Arg
NM_001382794.1:c.2317G>C	NP_001369723.1:p.Gly773Arg
NM_001382795.1:c.2311G>C	NP_001369724.1:p.Gly771Arg
NM_001382796.1:c.2359G>C	NP_001369725.1:p.Gly787Arg
NM_001382797.1:c.2260G>C	NP_001369726.1:p.Gly754Arg
NM_001382798.1:c.2359G>C	NP_001369727.1:p.Gly787Arg
NM_001382799.1:c.2179G>C	NP_001369728.1:p.Gly727Arg
NM_001382800.1:c.2308-272G>C	NP_001369729.1:n.2308-272G>C
NM_001382801.1:c.2311G>C	NP_001369730.1:p.Gly771Arg
NM_001382802.1:c.2101G>C	NP_001369731.1:p.Gly701Arg
NM_001382803.1:c.2317G>C	NP_001369732.1:p.Gly773Arg
NM_001382804.1:c.1531G>C	NP_001369733.1:p.Gly511Arg
NM_001382805.1:c.2208+1117G>C	NP_001369734.1:n.2208+1117G>C
NM_001382806.1:c.1321G>C	NP_001369735.1:p.Gly441Arg
NM_004448.4:c.2359G>C MANE Select	NP_004439.2:p.Gly787Arg
NR_110535.2:n.2597G>C