Canonical Allele Identifier: CA499890305

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143261825
• MyVariant Identifiers: chr17:g.37883799T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727546T>C , CM000679.2:g.39727546T>C	GRCh38
NC_000017.10:g.37883799T>C , CM000679.1:g.37883799T>C	GRCh37
NC_000017.9:g.35137325T>C	NCBI36
NG_007503.1:g.44407T>C , LRG_724:g.44407T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3411T>C MANE Select	ENSP00000269571.4:p.Pro1137=
ENST00000269571.9:c.3411T>C	ENSP00000269571.4:p.Pro1137=
ENST00000406381.6:c.3321T>C	ENSP00000385185.2:p.Pro1107=
ENST00000445658.6:c.2583T>C	ENSP00000404047.2:p.Pro861=
ENST00000541774.5:c.3366T>C	ENSP00000446466.1:p.Pro1122=
ENST00000578373.5:c.*3201T>C	ENSP00000463427.1:n.*3201T>C
ENST00000584450.5:c.3160-143T>C	ENSP00000463714.1:n.3160-143T>C
ENST00000584601.5:c.3321T>C	ENSP00000462438.1:p.Pro1107=
NM_001005862.2:c.3321T>C , LRG_724t1:c.3321T>C	NP_001005862.1:p.Pro1107=
NM_001289936.1:c.3366T>C , LRG_724t4:c.3366T>C	NP_001276865.1:p.Pro1122=
NM_001289937.1:c.3160-143T>C	NP_001276866.1:n.3160-143T>C
NM_004448.3:c.3411T>C , LRG_724t2:c.3411T>C	NP_004439.2:p.Pro1137=
NR_110535.1:n.3735T>C
XM_024450641.1:c.3549T>C	XP_024306409.1:p.Pro1183=
XM_024450642.1:c.3504T>C	XP_024306410.1:p.Pro1168=
XM_024450643.1:c.3459T>C	XP_024306411.1:p.Pro1153=
NM_001005862.3:c.3321T>C	NP_001005862.1:p.Pro1107=
NM_001289936.2:c.3366T>C	NP_001276865.1:p.Pro1122=
NM_001289937.2:c.3160-143T>C	NP_001276866.1:n.3160-143T>C
NM_001382782.1:c.3321T>C	NP_001369711.1:p.Pro1107=
NM_001382783.1:c.3321T>C	NP_001369712.1:p.Pro1107=
NM_001382784.1:c.3528T>C	NP_001369713.1:p.Pro1176=
NM_001382785.1:c.3513T>C	NP_001369714.1:p.Pro1171=
NM_001382786.1:c.3492T>C	NP_001369715.1:p.Pro1164=
NM_001382787.1:c.3486T>C	NP_001369716.1:p.Pro1162=
NM_001382788.1:c.3441T>C	NP_001369717.1:p.Pro1147=
NM_001382789.1:c.3432T>C	NP_001369718.1:p.Pro1144=
NM_001382790.1:c.3408T>C	NP_001369719.1:p.Pro1136=
NM_001382791.1:c.3402T>C	NP_001369720.1:p.Pro1134=
NM_001382792.1:c.3375T>C	NP_001369721.1:p.Pro1125=
NM_001382793.1:c.3369T>C	NP_001369722.1:p.Pro1123=
NM_001382794.1:c.3369T>C	NP_001369723.1:p.Pro1123=
NM_001382795.1:c.3363T>C	NP_001369724.1:p.Pro1121=
NM_001382796.1:c.3324T>C	NP_001369725.1:p.Pro1108=
NM_001382797.1:c.3312T>C	NP_001369726.1:p.Pro1104=
NM_001382798.1:c.3255T>C	NP_001369727.1:p.Pro1085=
NM_001382799.1:c.3231T>C	NP_001369728.1:p.Pro1077=
NM_001382800.1:c.3225T>C	NP_001369729.1:p.Pro1075=
NM_001382801.1:c.3207T>C	NP_001369730.1:p.Pro1069=
NM_001382802.1:c.3153T>C	NP_001369731.1:p.Pro1051=
NM_001382803.1:c.3118-143T>C	NP_001369732.1:n.3118-143T>C
NM_001382804.1:c.2583T>C	NP_001369733.1:p.Pro861=
NM_001382805.1:c.2460T>C	NP_001369734.1:p.Pro820=
NM_001382806.1:c.2373T>C	NP_001369735.1:p.Pro791=
NM_004448.4:c.3411T>C MANE Select	NP_004439.2:p.Pro1137=
NR_110535.2:n.3649T>C