Canonical Allele Identifier: CA399310947

Gene: ERBB2

Linked Data

• dbSNP Id: rs868797794
• MyVariant Identifiers: chr17:g.37883699A>C (hg19) ; chr17:g.39727446A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727446A>C , CM000679.2:g.39727446A>C	GRCh38
NC_000017.10:g.37883699A>C , CM000679.1:g.37883699A>C	GRCh37
NC_000017.9:g.35137225A>C	NCBI36
NG_007503.1:g.44307A>C , LRG_724:g.44307A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3311A>C MANE Select	ENSP00000269571.4:p.His1104Pro
ENST00000269571.9:c.3311A>C	ENSP00000269571.4:p.His1104Pro
ENST00000406381.6:c.3221A>C	ENSP00000385185.2:p.His1074Pro
ENST00000445658.6:c.2483A>C	ENSP00000404047.2:p.His828Pro
ENST00000541774.5:c.3266A>C	ENSP00000446466.1:p.His1089Pro
ENST00000578373.5:c.*3101A>C	ENSP00000463427.1:n.*3101A>C
ENST00000584450.5:c.3160-243A>C	ENSP00000463714.1:n.3160-243A>C
ENST00000584601.5:c.3221A>C	ENSP00000462438.1:p.His1074Pro
NM_001005862.2:c.3221A>C , LRG_724t1:c.3221A>C	NP_001005862.1:p.His1074Pro
NM_001289936.1:c.3266A>C , LRG_724t4:c.3266A>C	NP_001276865.1:p.His1089Pro
NM_001289937.1:c.3160-243A>C	NP_001276866.1:n.3160-243A>C
NM_004448.3:c.3311A>C , LRG_724t2:c.3311A>C	NP_004439.2:p.His1104Pro
NR_110535.1:n.3635A>C
XM_024450641.1:c.3449A>C	XP_024306409.1:p.His1150Pro
XM_024450642.1:c.3404A>C	XP_024306410.1:p.His1135Pro
XM_024450643.1:c.3359A>C	XP_024306411.1:p.His1120Pro
NM_001005862.3:c.3221A>C	NP_001005862.1:p.His1074Pro
NM_001289936.2:c.3266A>C	NP_001276865.1:p.His1089Pro
NM_001289937.2:c.3160-243A>C	NP_001276866.1:n.3160-243A>C
NM_001382782.1:c.3221A>C	NP_001369711.1:p.His1074Pro
NM_001382783.1:c.3221A>C	NP_001369712.1:p.His1074Pro
NM_001382784.1:c.3428A>C	NP_001369713.1:p.His1143Pro
NM_001382785.1:c.3413A>C	NP_001369714.1:p.His1138Pro
NM_001382786.1:c.3392A>C	NP_001369715.1:p.His1131Pro
NM_001382787.1:c.3386A>C	NP_001369716.1:p.His1129Pro
NM_001382788.1:c.3341A>C	NP_001369717.1:p.His1114Pro
NM_001382789.1:c.3332A>C	NP_001369718.1:p.His1111Pro
NM_001382790.1:c.3308A>C	NP_001369719.1:p.His1103Pro
NM_001382791.1:c.3302A>C	NP_001369720.1:p.His1101Pro
NM_001382792.1:c.3275A>C	NP_001369721.1:p.His1092Pro
NM_001382793.1:c.3269A>C	NP_001369722.1:p.His1090Pro
NM_001382794.1:c.3269A>C	NP_001369723.1:p.His1090Pro
NM_001382795.1:c.3263A>C	NP_001369724.1:p.His1088Pro
NM_001382796.1:c.3224A>C	NP_001369725.1:p.His1075Pro
NM_001382797.1:c.3212A>C	NP_001369726.1:p.His1071Pro
NM_001382798.1:c.3155A>C	NP_001369727.1:p.His1052Pro
NM_001382799.1:c.3131A>C	NP_001369728.1:p.His1044Pro
NM_001382800.1:c.3125A>C	NP_001369729.1:p.His1042Pro
NM_001382801.1:c.3107A>C	NP_001369730.1:p.His1036Pro
NM_001382802.1:c.3053A>C	NP_001369731.1:p.His1018Pro
NM_001382803.1:c.3118-243A>C	NP_001369732.1:n.3118-243A>C
NM_001382804.1:c.2483A>C	NP_001369733.1:p.His828Pro
NM_001382805.1:c.2360A>C	NP_001369734.1:p.His787Pro
NM_001382806.1:c.2273A>C	NP_001369735.1:p.His758Pro
NM_004448.4:c.3311A>C MANE Select	NP_004439.2:p.His1104Pro
NR_110535.2:n.3549A>C