Canonical Allele Identifier: CA399302826

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37880992T>C (hg19) ; chr17:g.39724739T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724739T>C , CM000679.2:g.39724739T>C	GRCh38
NC_000017.10:g.37880992T>C , CM000679.1:g.37880992T>C	GRCh37
NC_000017.9:g.35134518T>C	NCBI36
NG_007503.1:g.41600T>C , LRG_724:g.41600T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2321T>C MANE Select	ENSP00000269571.4:p.Met774Thr
ENST00000269571.9:c.2321T>C	ENSP00000269571.4:p.Met774Thr
ENST00000406381.6:c.2231T>C	ENSP00000385185.2:p.Met744Thr
ENST00000445658.6:c.1493T>C	ENSP00000404047.2:p.Met498Thr
ENST00000541774.5:c.2276T>C	ENSP00000446466.1:p.Met759Thr
ENST00000578373.5:c.*2111T>C	ENSP00000463427.1:n.*2111T>C
ENST00000580074.1:c.427T>C
ENST00000583038.5:n.3455T>C
ENST00000584450.5:c.2321T>C	ENSP00000463714.1:p.Met774Thr
ENST00000584601.5:c.2231T>C	ENSP00000462438.1:p.Met744Thr
NM_001005862.2:c.2231T>C , LRG_724t1:c.2231T>C	NP_001005862.1:p.Met744Thr
NM_001289936.1:c.2276T>C , LRG_724t4:c.2276T>C	NP_001276865.1:p.Met759Thr
NM_001289937.1:c.2321T>C	NP_001276866.1:p.Met774Thr
NM_004448.3:c.2321T>C , LRG_724t2:c.2321T>C	NP_004439.2:p.Met774Thr
NR_110535.1:n.2645T>C
XM_024450641.1:c.2459T>C	XP_024306409.1:p.Met820Thr
XM_024450642.1:c.2414T>C	XP_024306410.1:p.Met805Thr
XM_024450643.1:c.2369T>C	XP_024306411.1:p.Met790Thr
NM_001005862.3:c.2231T>C	NP_001005862.1:p.Met744Thr
NM_001289936.2:c.2276T>C	NP_001276865.1:p.Met759Thr
NM_001289937.2:c.2321T>C	NP_001276866.1:p.Met774Thr
NM_001382782.1:c.2231T>C	NP_001369711.1:p.Met744Thr
NM_001382783.1:c.2231T>C	NP_001369712.1:p.Met744Thr
NM_001382784.1:c.2438T>C	NP_001369713.1:p.Met813Thr
NM_001382785.1:c.2423T>C	NP_001369714.1:p.Met808Thr
NM_001382786.1:c.2402T>C	NP_001369715.1:p.Met801Thr
NM_001382787.1:c.2396T>C	NP_001369716.1:p.Met799Thr
NM_001382788.1:c.2351T>C	NP_001369717.1:p.Met784Thr
NM_001382789.1:c.2342T>C	NP_001369718.1:p.Met781Thr
NM_001382790.1:c.2318T>C	NP_001369719.1:p.Met773Thr
NM_001382791.1:c.2312T>C	NP_001369720.1:p.Met771Thr
NM_001382792.1:c.2285T>C	NP_001369721.1:p.Met762Thr
NM_001382793.1:c.2279T>C	NP_001369722.1:p.Met760Thr
NM_001382794.1:c.2279T>C	NP_001369723.1:p.Met760Thr
NM_001382795.1:c.2273T>C	NP_001369724.1:p.Met758Thr
NM_001382796.1:c.2321T>C	NP_001369725.1:p.Met774Thr
NM_001382797.1:c.2222T>C	NP_001369726.1:p.Met741Thr
NM_001382798.1:c.2321T>C	NP_001369727.1:p.Met774Thr
NM_001382799.1:c.2141T>C	NP_001369728.1:p.Met714Thr
NM_001382800.1:c.2308-310T>C	NP_001369729.1:n.2308-310T>C
NM_001382801.1:c.2273T>C	NP_001369730.1:p.Met758Thr
NM_001382802.1:c.2063T>C	NP_001369731.1:p.Met688Thr
NM_001382803.1:c.2279T>C	NP_001369732.1:p.Met760Thr
NM_001382804.1:c.1493T>C	NP_001369733.1:p.Met498Thr
NM_001382805.1:c.2208+1079T>C	NP_001369734.1:n.2208+1079T>C
NM_001382806.1:c.1283T>C	NP_001369735.1:p.Met428Thr
NM_004448.4:c.2321T>C MANE Select	NP_004439.2:p.Met774Thr
NR_110535.2:n.2559T>C