Canonical Allele Identifier: CA399304080

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145862173
• MyVariant Identifiers: chr17:g.37881307G>C (hg19) ; chr17:g.39725054G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725054G>C , CM000679.2:g.39725054G>C	GRCh38
NC_000017.10:g.37881307G>C , CM000679.1:g.37881307G>C	GRCh37
NC_000017.9:g.35134833G>C	NCBI36
NG_007503.1:g.41915G>C , LRG_724:g.41915G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2499G>C MANE Select	ENSP00000269571.4:p.Met833Ile
ENST00000269571.9:c.2499G>C	ENSP00000269571.4:p.Met833Ile
ENST00000406381.6:c.2409G>C	ENSP00000385185.2:p.Met803Ile
ENST00000445658.6:c.1671G>C	ENSP00000404047.2:p.Met557Ile
ENST00000541774.5:c.2454G>C	ENSP00000446466.1:p.Met818Ile
ENST00000578373.5:c.*2289G>C	ENSP00000463427.1:n.*2289G>C
ENST00000580074.1:c.605G>C
ENST00000583038.5:n.3633G>C
ENST00000584450.5:c.2499G>C	ENSP00000463714.1:p.Met833Ile
ENST00000584601.5:c.2409G>C	ENSP00000462438.1:p.Met803Ile
NM_001005862.2:c.2409G>C , LRG_724t1:c.2409G>C	NP_001005862.1:p.Met803Ile
NM_001289936.1:c.2454G>C , LRG_724t4:c.2454G>C	NP_001276865.1:p.Met818Ile
NM_001289937.1:c.2499G>C	NP_001276866.1:p.Met833Ile
NM_004448.3:c.2499G>C , LRG_724t2:c.2499G>C	NP_004439.2:p.Met833Ile
NR_110535.1:n.2823G>C
XM_024450641.1:c.2637G>C	XP_024306409.1:p.Met879Ile
XM_024450642.1:c.2592G>C	XP_024306410.1:p.Met864Ile
XM_024450643.1:c.2547G>C	XP_024306411.1:p.Met849Ile
NM_001005862.3:c.2409G>C	NP_001005862.1:p.Met803Ile
NM_001289936.2:c.2454G>C	NP_001276865.1:p.Met818Ile
NM_001289937.2:c.2499G>C	NP_001276866.1:p.Met833Ile
NM_001382782.1:c.2409G>C	NP_001369711.1:p.Met803Ile
NM_001382783.1:c.2409G>C	NP_001369712.1:p.Met803Ile
NM_001382784.1:c.2616G>C	NP_001369713.1:p.Met872Ile
NM_001382785.1:c.2601G>C	NP_001369714.1:p.Met867Ile
NM_001382786.1:c.2580G>C	NP_001369715.1:p.Met860Ile
NM_001382787.1:c.2574G>C	NP_001369716.1:p.Met858Ile
NM_001382788.1:c.2529G>C	NP_001369717.1:p.Met843Ile
NM_001382789.1:c.2520G>C	NP_001369718.1:p.Met840Ile
NM_001382790.1:c.2496G>C	NP_001369719.1:p.Met832Ile
NM_001382791.1:c.2490G>C	NP_001369720.1:p.Met830Ile
NM_001382792.1:c.2463G>C	NP_001369721.1:p.Met821Ile
NM_001382793.1:c.2457G>C	NP_001369722.1:p.Met819Ile
NM_001382794.1:c.2457G>C	NP_001369723.1:p.Met819Ile
NM_001382795.1:c.2451G>C	NP_001369724.1:p.Met817Ile
NM_001382796.1:c.2499G>C	NP_001369725.1:p.Met833Ile
NM_001382797.1:c.2400G>C	NP_001369726.1:p.Met800Ile
NM_001382798.1:c.2493+143G>C	NP_001369727.1:n.2493+143G>C
NM_001382799.1:c.2319G>C	NP_001369728.1:p.Met773Ile
NM_001382800.1:c.2313G>C	NP_001369729.1:p.Met771Ile
NM_001382801.1:c.2445+143G>C	NP_001369730.1:n.2445+143G>C
NM_001382802.1:c.2241G>C	NP_001369731.1:p.Met747Ile
NM_001382803.1:c.2457G>C	NP_001369732.1:p.Met819Ile
NM_001382804.1:c.1671G>C	NP_001369733.1:p.Met557Ile
NM_001382805.1:c.2208+1394G>C	NP_001369734.1:n.2208+1394G>C
NM_001382806.1:c.1461G>C	NP_001369735.1:p.Met487Ile
NM_004448.4:c.2499G>C MANE Select	NP_004439.2:p.Met833Ile
NR_110535.2:n.2737G>C