Canonical Allele Identifier: CA399304077

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145862133
• MyVariant Identifiers: chr17:g.37881306T>C (hg19) ; chr17:g.39725053T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725053T>C , CM000679.2:g.39725053T>C	GRCh38
NC_000017.10:g.37881306T>C , CM000679.1:g.37881306T>C	GRCh37
NC_000017.9:g.35134832T>C	NCBI36
NG_007503.1:g.41914T>C , LRG_724:g.41914T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2498T>C MANE Select	ENSP00000269571.4:p.Met833Thr
ENST00000269571.9:c.2498T>C	ENSP00000269571.4:p.Met833Thr
ENST00000406381.6:c.2408T>C	ENSP00000385185.2:p.Met803Thr
ENST00000445658.6:c.1670T>C	ENSP00000404047.2:p.Met557Thr
ENST00000541774.5:c.2453T>C	ENSP00000446466.1:p.Met818Thr
ENST00000578373.5:c.*2288T>C	ENSP00000463427.1:n.*2288T>C
ENST00000580074.1:c.604T>C
ENST00000583038.5:n.3632T>C
ENST00000584450.5:c.2498T>C	ENSP00000463714.1:p.Met833Thr
ENST00000584601.5:c.2408T>C	ENSP00000462438.1:p.Met803Thr
NM_001005862.2:c.2408T>C , LRG_724t1:c.2408T>C	NP_001005862.1:p.Met803Thr
NM_001289936.1:c.2453T>C , LRG_724t4:c.2453T>C	NP_001276865.1:p.Met818Thr
NM_001289937.1:c.2498T>C	NP_001276866.1:p.Met833Thr
NM_004448.3:c.2498T>C , LRG_724t2:c.2498T>C	NP_004439.2:p.Met833Thr
NR_110535.1:n.2822T>C
XM_024450641.1:c.2636T>C	XP_024306409.1:p.Met879Thr
XM_024450642.1:c.2591T>C	XP_024306410.1:p.Met864Thr
XM_024450643.1:c.2546T>C	XP_024306411.1:p.Met849Thr
NM_001005862.3:c.2408T>C	NP_001005862.1:p.Met803Thr
NM_001289936.2:c.2453T>C	NP_001276865.1:p.Met818Thr
NM_001289937.2:c.2498T>C	NP_001276866.1:p.Met833Thr
NM_001382782.1:c.2408T>C	NP_001369711.1:p.Met803Thr
NM_001382783.1:c.2408T>C	NP_001369712.1:p.Met803Thr
NM_001382784.1:c.2615T>C	NP_001369713.1:p.Met872Thr
NM_001382785.1:c.2600T>C	NP_001369714.1:p.Met867Thr
NM_001382786.1:c.2579T>C	NP_001369715.1:p.Met860Thr
NM_001382787.1:c.2573T>C	NP_001369716.1:p.Met858Thr
NM_001382788.1:c.2528T>C	NP_001369717.1:p.Met843Thr
NM_001382789.1:c.2519T>C	NP_001369718.1:p.Met840Thr
NM_001382790.1:c.2495T>C	NP_001369719.1:p.Met832Thr
NM_001382791.1:c.2489T>C	NP_001369720.1:p.Met830Thr
NM_001382792.1:c.2462T>C	NP_001369721.1:p.Met821Thr
NM_001382793.1:c.2456T>C	NP_001369722.1:p.Met819Thr
NM_001382794.1:c.2456T>C	NP_001369723.1:p.Met819Thr
NM_001382795.1:c.2450T>C	NP_001369724.1:p.Met817Thr
NM_001382796.1:c.2498T>C	NP_001369725.1:p.Met833Thr
NM_001382797.1:c.2399T>C	NP_001369726.1:p.Met800Thr
NM_001382798.1:c.2493+142T>C	NP_001369727.1:n.2493+142T>C
NM_001382799.1:c.2318T>C	NP_001369728.1:p.Met773Thr
NM_001382800.1:c.2312T>C	NP_001369729.1:p.Met771Thr
NM_001382801.1:c.2445+142T>C	NP_001369730.1:n.2445+142T>C
NM_001382802.1:c.2240T>C	NP_001369731.1:p.Met747Thr
NM_001382803.1:c.2456T>C	NP_001369732.1:p.Met819Thr
NM_001382804.1:c.1670T>C	NP_001369733.1:p.Met557Thr
NM_001382805.1:c.2208+1393T>C	NP_001369734.1:n.2208+1393T>C
NM_001382806.1:c.1460T>C	NP_001369735.1:p.Met487Thr
NM_004448.4:c.2498T>C MANE Select	NP_004439.2:p.Met833Thr
NR_110535.2:n.2736T>C