Canonical Allele Identifier: CA399303362

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145851274
• MyVariant Identifiers: chr17:g.37881085G>C (hg19) ; chr17:g.39724832G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724832G>C , CM000679.2:g.39724832G>C	GRCh38
NC_000017.10:g.37881085G>C , CM000679.1:g.37881085G>C	GRCh37
NC_000017.9:g.35134611G>C	NCBI36
NG_007503.1:g.41693G>C , LRG_724:g.41693G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2414G>C MANE Select	ENSP00000269571.4:p.Cys805Ser
ENST00000269571.9:c.2414G>C	ENSP00000269571.4:p.Cys805Ser
ENST00000406381.6:c.2324G>C	ENSP00000385185.2:p.Cys775Ser
ENST00000445658.6:c.1586G>C	ENSP00000404047.2:p.Cys529Ser
ENST00000541774.5:c.2369G>C	ENSP00000446466.1:p.Cys790Ser
ENST00000578373.5:c.*2204G>C	ENSP00000463427.1:n.*2204G>C
ENST00000580074.1:c.520G>C
ENST00000583038.5:n.3548G>C
ENST00000584450.5:c.2414G>C	ENSP00000463714.1:p.Cys805Ser
ENST00000584601.5:c.2324G>C	ENSP00000462438.1:p.Cys775Ser
NM_001005862.2:c.2324G>C , LRG_724t1:c.2324G>C	NP_001005862.1:p.Cys775Ser
NM_001289936.1:c.2369G>C , LRG_724t4:c.2369G>C	NP_001276865.1:p.Cys790Ser
NM_001289937.1:c.2414G>C	NP_001276866.1:p.Cys805Ser
NM_004448.3:c.2414G>C , LRG_724t2:c.2414G>C	NP_004439.2:p.Cys805Ser
NR_110535.1:n.2738G>C
XM_024450641.1:c.2552G>C	XP_024306409.1:p.Cys851Ser
XM_024450642.1:c.2507G>C	XP_024306410.1:p.Cys836Ser
XM_024450643.1:c.2462G>C	XP_024306411.1:p.Cys821Ser
NM_001005862.3:c.2324G>C	NP_001005862.1:p.Cys775Ser
NM_001289936.2:c.2369G>C	NP_001276865.1:p.Cys790Ser
NM_001289937.2:c.2414G>C	NP_001276866.1:p.Cys805Ser
NM_001382782.1:c.2324G>C	NP_001369711.1:p.Cys775Ser
NM_001382783.1:c.2324G>C	NP_001369712.1:p.Cys775Ser
NM_001382784.1:c.2531G>C	NP_001369713.1:p.Cys844Ser
NM_001382785.1:c.2516G>C	NP_001369714.1:p.Cys839Ser
NM_001382786.1:c.2495G>C	NP_001369715.1:p.Cys832Ser
NM_001382787.1:c.2489G>C	NP_001369716.1:p.Cys830Ser
NM_001382788.1:c.2444G>C	NP_001369717.1:p.Cys815Ser
NM_001382789.1:c.2435G>C	NP_001369718.1:p.Cys812Ser
NM_001382790.1:c.2411G>C	NP_001369719.1:p.Cys804Ser
NM_001382791.1:c.2405G>C	NP_001369720.1:p.Cys802Ser
NM_001382792.1:c.2378G>C	NP_001369721.1:p.Cys793Ser
NM_001382793.1:c.2372G>C	NP_001369722.1:p.Cys791Ser
NM_001382794.1:c.2372G>C	NP_001369723.1:p.Cys791Ser
NM_001382795.1:c.2366G>C	NP_001369724.1:p.Cys789Ser
NM_001382796.1:c.2414G>C	NP_001369725.1:p.Cys805Ser
NM_001382797.1:c.2315G>C	NP_001369726.1:p.Cys772Ser
NM_001382798.1:c.2414G>C	NP_001369727.1:p.Cys805Ser
NM_001382799.1:c.2234G>C	NP_001369728.1:p.Cys745Ser
NM_001382800.1:c.2308-217G>C	NP_001369729.1:n.2308-217G>C
NM_001382801.1:c.2366G>C	NP_001369730.1:p.Cys789Ser
NM_001382802.1:c.2156G>C	NP_001369731.1:p.Cys719Ser
NM_001382803.1:c.2372G>C	NP_001369732.1:p.Cys791Ser
NM_001382804.1:c.1586G>C	NP_001369733.1:p.Cys529Ser
NM_001382805.1:c.2208+1172G>C	NP_001369734.1:n.2208+1172G>C
NM_001382806.1:c.1376G>C	NP_001369735.1:p.Cys459Ser
NM_004448.4:c.2414G>C MANE Select	NP_004439.2:p.Cys805Ser
NR_110535.2:n.2652G>C