Canonical Allele Identifier: CA399310573

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883645T>C (hg19) ; chr17:g.39727392T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727392T>C , CM000679.2:g.39727392T>C	GRCh38
NC_000017.10:g.37883645T>C , CM000679.1:g.37883645T>C	GRCh37
NC_000017.9:g.35137171T>C	NCBI36
NG_007503.1:g.44253T>C , LRG_724:g.44253T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3257T>C MANE Select	ENSP00000269571.4:p.Phe1086Ser
ENST00000269571.9:c.3257T>C	ENSP00000269571.4:p.Phe1086Ser
ENST00000406381.6:c.3167T>C	ENSP00000385185.2:p.Phe1056Ser
ENST00000445658.6:c.2429T>C	ENSP00000404047.2:p.Phe810Ser
ENST00000541774.5:c.3212T>C	ENSP00000446466.1:p.Phe1071Ser
ENST00000578373.5:c.*3047T>C	ENSP00000463427.1:n.*3047T>C
ENST00000584450.5:c.3160-297T>C	ENSP00000463714.1:n.3160-297T>C
ENST00000584601.5:c.3167T>C	ENSP00000462438.1:p.Phe1056Ser
NM_001005862.2:c.3167T>C , LRG_724t1:c.3167T>C	NP_001005862.1:p.Phe1056Ser
NM_001289936.1:c.3212T>C , LRG_724t4:c.3212T>C	NP_001276865.1:p.Phe1071Ser
NM_001289937.1:c.3160-297T>C	NP_001276866.1:n.3160-297T>C
NM_004448.3:c.3257T>C , LRG_724t2:c.3257T>C	NP_004439.2:p.Phe1086Ser
NR_110535.1:n.3581T>C
XM_024450641.1:c.3395T>C	XP_024306409.1:p.Phe1132Ser
XM_024450642.1:c.3350T>C	XP_024306410.1:p.Phe1117Ser
XM_024450643.1:c.3305T>C	XP_024306411.1:p.Phe1102Ser
NM_001005862.3:c.3167T>C	NP_001005862.1:p.Phe1056Ser
NM_001289936.2:c.3212T>C	NP_001276865.1:p.Phe1071Ser
NM_001289937.2:c.3160-297T>C	NP_001276866.1:n.3160-297T>C
NM_001382782.1:c.3167T>C	NP_001369711.1:p.Phe1056Ser
NM_001382783.1:c.3167T>C	NP_001369712.1:p.Phe1056Ser
NM_001382784.1:c.3374T>C	NP_001369713.1:p.Phe1125Ser
NM_001382785.1:c.3359T>C	NP_001369714.1:p.Phe1120Ser
NM_001382786.1:c.3338T>C	NP_001369715.1:p.Phe1113Ser
NM_001382787.1:c.3332T>C	NP_001369716.1:p.Phe1111Ser
NM_001382788.1:c.3287T>C	NP_001369717.1:p.Phe1096Ser
NM_001382789.1:c.3278T>C	NP_001369718.1:p.Phe1093Ser
NM_001382790.1:c.3254T>C	NP_001369719.1:p.Phe1085Ser
NM_001382791.1:c.3248T>C	NP_001369720.1:p.Phe1083Ser
NM_001382792.1:c.3221T>C	NP_001369721.1:p.Phe1074Ser
NM_001382793.1:c.3215T>C	NP_001369722.1:p.Phe1072Ser
NM_001382794.1:c.3215T>C	NP_001369723.1:p.Phe1072Ser
NM_001382795.1:c.3209T>C	NP_001369724.1:p.Phe1070Ser
NM_001382796.1:c.3170T>C	NP_001369725.1:p.Phe1057Ser
NM_001382797.1:c.3158T>C	NP_001369726.1:p.Phe1053Ser
NM_001382798.1:c.3101T>C	NP_001369727.1:p.Phe1034Ser
NM_001382799.1:c.3077T>C	NP_001369728.1:p.Phe1026Ser
NM_001382800.1:c.3071T>C	NP_001369729.1:p.Phe1024Ser
NM_001382801.1:c.3053T>C	NP_001369730.1:p.Phe1018Ser
NM_001382802.1:c.2999T>C	NP_001369731.1:p.Phe1000Ser
NM_001382803.1:c.3118-297T>C	NP_001369732.1:n.3118-297T>C
NM_001382804.1:c.2429T>C	NP_001369733.1:p.Phe810Ser
NM_001382805.1:c.2306T>C	NP_001369734.1:p.Phe769Ser
NM_001382806.1:c.2219T>C	NP_001369735.1:p.Phe740Ser
NM_004448.4:c.3257T>C MANE Select	NP_004439.2:p.Phe1086Ser
NR_110535.2:n.3495T>C