Canonical Allele Identifier: CA499890302

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143261192
• MyVariant Identifiers: chr17:g.37883793C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727540C>T , CM000679.2:g.39727540C>T	GRCh38
NC_000017.10:g.37883793C>T , CM000679.1:g.37883793C>T	GRCh37
NC_000017.9:g.35137319C>T	NCBI36
NG_007503.1:g.44401C>T , LRG_724:g.44401C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3405C>T MANE Select	ENSP00000269571.4:p.Pro1135=
ENST00000269571.9:c.3405C>T	ENSP00000269571.4:p.Pro1135=
ENST00000406381.6:c.3315C>T	ENSP00000385185.2:p.Pro1105=
ENST00000445658.6:c.2577C>T	ENSP00000404047.2:p.Pro859=
ENST00000541774.5:c.3360C>T	ENSP00000446466.1:p.Pro1120=
ENST00000578373.5:c.*3195C>T	ENSP00000463427.1:n.*3195C>T
ENST00000584450.5:c.3160-149C>T	ENSP00000463714.1:n.3160-149C>T
ENST00000584601.5:c.3315C>T	ENSP00000462438.1:p.Pro1105=
NM_001005862.2:c.3315C>T , LRG_724t1:c.3315C>T	NP_001005862.1:p.Pro1105=
NM_001289936.1:c.3360C>T , LRG_724t4:c.3360C>T	NP_001276865.1:p.Pro1120=
NM_001289937.1:c.3160-149C>T	NP_001276866.1:n.3160-149C>T
NM_004448.3:c.3405C>T , LRG_724t2:c.3405C>T	NP_004439.2:p.Pro1135=
NR_110535.1:n.3729C>T
XM_024450641.1:c.3543C>T	XP_024306409.1:p.Pro1181=
XM_024450642.1:c.3498C>T	XP_024306410.1:p.Pro1166=
XM_024450643.1:c.3453C>T	XP_024306411.1:p.Pro1151=
NM_001005862.3:c.3315C>T	NP_001005862.1:p.Pro1105=
NM_001289936.2:c.3360C>T	NP_001276865.1:p.Pro1120=
NM_001289937.2:c.3160-149C>T	NP_001276866.1:n.3160-149C>T
NM_001382782.1:c.3315C>T	NP_001369711.1:p.Pro1105=
NM_001382783.1:c.3315C>T	NP_001369712.1:p.Pro1105=
NM_001382784.1:c.3522C>T	NP_001369713.1:p.Pro1174=
NM_001382785.1:c.3507C>T	NP_001369714.1:p.Pro1169=
NM_001382786.1:c.3486C>T	NP_001369715.1:p.Pro1162=
NM_001382787.1:c.3480C>T	NP_001369716.1:p.Pro1160=
NM_001382788.1:c.3435C>T	NP_001369717.1:p.Pro1145=
NM_001382789.1:c.3426C>T	NP_001369718.1:p.Pro1142=
NM_001382790.1:c.3402C>T	NP_001369719.1:p.Pro1134=
NM_001382791.1:c.3396C>T	NP_001369720.1:p.Pro1132=
NM_001382792.1:c.3369C>T	NP_001369721.1:p.Pro1123=
NM_001382793.1:c.3363C>T	NP_001369722.1:p.Pro1121=
NM_001382794.1:c.3363C>T	NP_001369723.1:p.Pro1121=
NM_001382795.1:c.3357C>T	NP_001369724.1:p.Pro1119=
NM_001382796.1:c.3318C>T	NP_001369725.1:p.Pro1106=
NM_001382797.1:c.3306C>T	NP_001369726.1:p.Pro1102=
NM_001382798.1:c.3249C>T	NP_001369727.1:p.Pro1083=
NM_001382799.1:c.3225C>T	NP_001369728.1:p.Pro1075=
NM_001382800.1:c.3219C>T	NP_001369729.1:p.Pro1073=
NM_001382801.1:c.3201C>T	NP_001369730.1:p.Pro1067=
NM_001382802.1:c.3147C>T	NP_001369731.1:p.Pro1049=
NM_001382803.1:c.3118-149C>T	NP_001369732.1:n.3118-149C>T
NM_001382804.1:c.2577C>T	NP_001369733.1:p.Pro859=
NM_001382805.1:c.2454C>T	NP_001369734.1:p.Pro818=
NM_001382806.1:c.2367C>T	NP_001369735.1:p.Pro789=
NM_004448.4:c.3405C>T MANE Select	NP_004439.2:p.Pro1135=
NR_110535.2:n.3643C>T