Canonical Allele Identifier: CA399313544

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143301685
• MyVariant Identifiers: chr17:g.37884083T>C (hg19) ; chr17:g.39727830T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727830T>C , CM000679.2:g.39727830T>C	GRCh38
NC_000017.10:g.37884083T>C , CM000679.1:g.37884083T>C	GRCh37
NC_000017.9:g.35137609T>C	NCBI36
NG_007503.1:g.44691T>C , LRG_724:g.44691T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3554T>C MANE Select	ENSP00000269571.4:p.Phe1185Ser
ENST00000269571.9:c.3554T>C	ENSP00000269571.4:p.Phe1185Ser
ENST00000406381.6:c.3464T>C	ENSP00000385185.2:p.Phe1155Ser
ENST00000445658.6:c.2726T>C	ENSP00000404047.2:p.Phe909Ser
ENST00000541774.5:c.3509T>C	ENSP00000446466.1:p.Phe1170Ser
ENST00000578373.5:c.*3344T>C	ENSP00000463427.1:n.*3344T>C
ENST00000584450.5:c.*133T>C	ENSP00000463714.1:n.*133T>C
ENST00000584601.5:c.3464T>C	ENSP00000462438.1:p.Phe1155Ser
NM_001005862.2:c.3464T>C , LRG_724t1:c.3464T>C	NP_001005862.1:p.Phe1155Ser
NM_001289936.1:c.3509T>C , LRG_724t4:c.3509T>C	NP_001276865.1:p.Phe1170Ser
NM_001289937.1:c.*133T>C	NP_001276866.1:n.*133T>C
NM_004448.3:c.3554T>C , LRG_724t2:c.3554T>C	NP_004439.2:p.Phe1185Ser
NR_110535.1:n.3878T>C
XM_024450641.1:c.3692T>C	XP_024306409.1:p.Phe1231Ser
XM_024450642.1:c.3647T>C	XP_024306410.1:p.Phe1216Ser
XM_024450643.1:c.3602T>C	XP_024306411.1:p.Phe1201Ser
NM_001005862.3:c.3464T>C	NP_001005862.1:p.Phe1155Ser
NM_001289936.2:c.3509T>C	NP_001276865.1:p.Phe1170Ser
NM_001289937.2:c.*133T>C	NP_001276866.1:n.*133T>C
NM_001382782.1:c.3464T>C	NP_001369711.1:p.Phe1155Ser
NM_001382783.1:c.3464T>C	NP_001369712.1:p.Phe1155Ser
NM_001382784.1:c.3671T>C	NP_001369713.1:p.Phe1224Ser
NM_001382785.1:c.3656T>C	NP_001369714.1:p.Phe1219Ser
NM_001382786.1:c.3635T>C	NP_001369715.1:p.Phe1212Ser
NM_001382787.1:c.3629T>C	NP_001369716.1:p.Phe1210Ser
NM_001382788.1:c.3584T>C	NP_001369717.1:p.Phe1195Ser
NM_001382789.1:c.3575T>C	NP_001369718.1:p.Phe1192Ser
NM_001382790.1:c.3551T>C	NP_001369719.1:p.Phe1184Ser
NM_001382791.1:c.3545T>C	NP_001369720.1:p.Phe1182Ser
NM_001382792.1:c.3518T>C	NP_001369721.1:p.Phe1173Ser
NM_001382793.1:c.3512T>C	NP_001369722.1:p.Phe1171Ser
NM_001382794.1:c.3512T>C	NP_001369723.1:p.Phe1171Ser
NM_001382795.1:c.3506T>C	NP_001369724.1:p.Phe1169Ser
NM_001382796.1:c.3467T>C	NP_001369725.1:p.Phe1156Ser
NM_001382797.1:c.3455T>C	NP_001369726.1:p.Phe1152Ser
NM_001382798.1:c.3398T>C	NP_001369727.1:p.Phe1133Ser
NM_001382799.1:c.3374T>C	NP_001369728.1:p.Phe1125Ser
NM_001382800.1:c.3368T>C	NP_001369729.1:p.Phe1123Ser
NM_001382801.1:c.3350T>C	NP_001369730.1:p.Phe1117Ser
NM_001382802.1:c.3296T>C	NP_001369731.1:p.Phe1099Ser
NM_001382803.1:c.*133T>C	NP_001369732.1:n.*133T>C
NM_001382804.1:c.2726T>C	NP_001369733.1:p.Phe909Ser
NM_001382805.1:c.2603T>C	NP_001369734.1:p.Phe868Ser
NM_001382806.1:c.2516T>C	NP_001369735.1:p.Phe839Ser
NM_004448.4:c.3554T>C MANE Select	NP_004439.2:p.Phe1185Ser
NR_110535.2:n.3792T>C