Canonical Allele Identifier: CA399304367

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145863613
• MyVariant Identifiers: chr17:g.37881341G>C (hg19) ; chr17:g.39725088G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725088G>C , CM000679.2:g.39725088G>C	GRCh38
NC_000017.10:g.37881341G>C , CM000679.1:g.37881341G>C	GRCh37
NC_000017.9:g.35134867G>C	NCBI36
NG_007503.1:g.41949G>C , LRG_724:g.41949G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2533G>C MANE Select	ENSP00000269571.4:p.Asp845His
ENST00000269571.9:c.2533G>C	ENSP00000269571.4:p.Asp845His
ENST00000406381.6:c.2443G>C	ENSP00000385185.2:p.Asp815His
ENST00000445658.6:c.1705G>C	ENSP00000404047.2:p.Asp569His
ENST00000541774.5:c.2488G>C	ENSP00000446466.1:p.Asp830His
ENST00000578373.5:c.*2323G>C	ENSP00000463427.1:n.*2323G>C
ENST00000580074.1:c.639G>C
ENST00000583038.5:n.3667G>C
ENST00000584450.5:c.2533G>C	ENSP00000463714.1:p.Asp845His
ENST00000584601.5:c.2443G>C	ENSP00000462438.1:p.Asp815His
NM_001005862.2:c.2443G>C , LRG_724t1:c.2443G>C	NP_001005862.1:p.Asp815His
NM_001289936.1:c.2488G>C , LRG_724t4:c.2488G>C	NP_001276865.1:p.Asp830His
NM_001289937.1:c.2533G>C	NP_001276866.1:p.Asp845His
NM_004448.3:c.2533G>C , LRG_724t2:c.2533G>C	NP_004439.2:p.Asp845His
NR_110535.1:n.2857G>C
XM_024450641.1:c.2671G>C	XP_024306409.1:p.Asp891His
XM_024450642.1:c.2626G>C	XP_024306410.1:p.Asp876His
XM_024450643.1:c.2581G>C	XP_024306411.1:p.Asp861His
NM_001005862.3:c.2443G>C	NP_001005862.1:p.Asp815His
NM_001289936.2:c.2488G>C	NP_001276865.1:p.Asp830His
NM_001289937.2:c.2533G>C	NP_001276866.1:p.Asp845His
NM_001382782.1:c.2443G>C	NP_001369711.1:p.Asp815His
NM_001382783.1:c.2443G>C	NP_001369712.1:p.Asp815His
NM_001382784.1:c.2650G>C	NP_001369713.1:p.Asp884His
NM_001382785.1:c.2635G>C	NP_001369714.1:p.Asp879His
NM_001382786.1:c.2614G>C	NP_001369715.1:p.Asp872His
NM_001382787.1:c.2608G>C	NP_001369716.1:p.Asp870His
NM_001382788.1:c.2563G>C	NP_001369717.1:p.Asp855His
NM_001382789.1:c.2554G>C	NP_001369718.1:p.Asp852His
NM_001382790.1:c.2530G>C	NP_001369719.1:p.Asp844His
NM_001382791.1:c.2524G>C	NP_001369720.1:p.Asp842His
NM_001382792.1:c.2497G>C	NP_001369721.1:p.Asp833His
NM_001382793.1:c.2491G>C	NP_001369722.1:p.Asp831His
NM_001382794.1:c.2491G>C	NP_001369723.1:p.Asp831His
NM_001382795.1:c.2485G>C	NP_001369724.1:p.Asp829His
NM_001382796.1:c.2533G>C	NP_001369725.1:p.Asp845His
NM_001382797.1:c.2434G>C	NP_001369726.1:p.Asp812His
NM_001382798.1:c.2493+177G>C	NP_001369727.1:n.2493+177G>C
NM_001382799.1:c.2353G>C	NP_001369728.1:p.Asp785His
NM_001382800.1:c.2347G>C	NP_001369729.1:p.Asp783His
NM_001382801.1:c.2445+177G>C	NP_001369730.1:n.2445+177G>C
NM_001382802.1:c.2275G>C	NP_001369731.1:p.Asp759His
NM_001382803.1:c.2491G>C	NP_001369732.1:p.Asp831His
NM_001382804.1:c.1705G>C	NP_001369733.1:p.Asp569His
NM_001382805.1:c.2208+1428G>C	NP_001369734.1:n.2208+1428G>C
NM_001382806.1:c.1495G>C	NP_001369735.1:p.Asp499His
NM_004448.4:c.2533G>C MANE Select	NP_004439.2:p.Asp845His
NR_110535.2:n.2771G>C