Canonical Allele Identifier: CA399310493

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143241411
• MyVariant Identifiers: chr17:g.37883633G>C (hg19) ; chr17:g.39727380G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727380G>C , CM000679.2:g.39727380G>C	GRCh38
NC_000017.10:g.37883633G>C , CM000679.1:g.37883633G>C	GRCh37
NC_000017.9:g.35137159G>C	NCBI36
NG_007503.1:g.44241G>C , LRG_724:g.44241G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3245G>C MANE Select	ENSP00000269571.4:p.Gly1082Ala
ENST00000269571.9:c.3245G>C	ENSP00000269571.4:p.Gly1082Ala
ENST00000406381.6:c.3155G>C	ENSP00000385185.2:p.Gly1052Ala
ENST00000445658.6:c.2417G>C	ENSP00000404047.2:p.Gly806Ala
ENST00000541774.5:c.3200G>C	ENSP00000446466.1:p.Gly1067Ala
ENST00000578373.5:c.*3035G>C	ENSP00000463427.1:n.*3035G>C
ENST00000584450.5:c.3160-309G>C	ENSP00000463714.1:n.3160-309G>C
ENST00000584601.5:c.3155G>C	ENSP00000462438.1:p.Gly1052Ala
NM_001005862.2:c.3155G>C , LRG_724t1:c.3155G>C	NP_001005862.1:p.Gly1052Ala
NM_001289936.1:c.3200G>C , LRG_724t4:c.3200G>C	NP_001276865.1:p.Gly1067Ala
NM_001289937.1:c.3160-309G>C	NP_001276866.1:n.3160-309G>C
NM_004448.3:c.3245G>C , LRG_724t2:c.3245G>C	NP_004439.2:p.Gly1082Ala
NR_110535.1:n.3569G>C
XM_024450641.1:c.3383G>C	XP_024306409.1:p.Gly1128Ala
XM_024450642.1:c.3338G>C	XP_024306410.1:p.Gly1113Ala
XM_024450643.1:c.3293G>C	XP_024306411.1:p.Gly1098Ala
NM_001005862.3:c.3155G>C	NP_001005862.1:p.Gly1052Ala
NM_001289936.2:c.3200G>C	NP_001276865.1:p.Gly1067Ala
NM_001289937.2:c.3160-309G>C	NP_001276866.1:n.3160-309G>C
NM_001382782.1:c.3155G>C	NP_001369711.1:p.Gly1052Ala
NM_001382783.1:c.3155G>C	NP_001369712.1:p.Gly1052Ala
NM_001382784.1:c.3362G>C	NP_001369713.1:p.Gly1121Ala
NM_001382785.1:c.3347G>C	NP_001369714.1:p.Gly1116Ala
NM_001382786.1:c.3326G>C	NP_001369715.1:p.Gly1109Ala
NM_001382787.1:c.3320G>C	NP_001369716.1:p.Gly1107Ala
NM_001382788.1:c.3275G>C	NP_001369717.1:p.Gly1092Ala
NM_001382789.1:c.3266G>C	NP_001369718.1:p.Gly1089Ala
NM_001382790.1:c.3242G>C	NP_001369719.1:p.Gly1081Ala
NM_001382791.1:c.3236G>C	NP_001369720.1:p.Gly1079Ala
NM_001382792.1:c.3209G>C	NP_001369721.1:p.Gly1070Ala
NM_001382793.1:c.3203G>C	NP_001369722.1:p.Gly1068Ala
NM_001382794.1:c.3203G>C	NP_001369723.1:p.Gly1068Ala
NM_001382795.1:c.3197G>C	NP_001369724.1:p.Gly1066Ala
NM_001382796.1:c.3158G>C	NP_001369725.1:p.Gly1053Ala
NM_001382797.1:c.3146G>C	NP_001369726.1:p.Gly1049Ala
NM_001382798.1:c.3089G>C	NP_001369727.1:p.Gly1030Ala
NM_001382799.1:c.3065G>C	NP_001369728.1:p.Gly1022Ala
NM_001382800.1:c.3059G>C	NP_001369729.1:p.Gly1020Ala
NM_001382801.1:c.3041G>C	NP_001369730.1:p.Gly1014Ala
NM_001382802.1:c.2987G>C	NP_001369731.1:p.Gly996Ala
NM_001382803.1:c.3118-309G>C	NP_001369732.1:n.3118-309G>C
NM_001382804.1:c.2417G>C	NP_001369733.1:p.Gly806Ala
NM_001382805.1:c.2294G>C	NP_001369734.1:p.Gly765Ala
NM_001382806.1:c.2207G>C	NP_001369735.1:p.Gly736Ala
NM_004448.4:c.3245G>C MANE Select	NP_004439.2:p.Gly1082Ala
NR_110535.2:n.3483G>C