Canonical Allele Identifier: CA499890636

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884024C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727771C>A , CM000679.2:g.39727771C>A	GRCh38
NC_000017.10:g.37884024C>A , CM000679.1:g.37884024C>A	GRCh37
NC_000017.9:g.35137550C>A	NCBI36
NG_007503.1:g.44632C>A , LRG_724:g.44632C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3495C>A MANE Select	ENSP00000269571.4:p.Ala1165=
ENST00000269571.9:c.3495C>A	ENSP00000269571.4:p.Ala1165=
ENST00000406381.6:c.3405C>A	ENSP00000385185.2:p.Ala1135=
ENST00000445658.6:c.2667C>A	ENSP00000404047.2:p.Ala889=
ENST00000541774.5:c.3450C>A	ENSP00000446466.1:p.Ala1150=
ENST00000578373.5:c.*3285C>A	ENSP00000463427.1:n.*3285C>A
ENST00000584450.5:c.*74C>A	ENSP00000463714.1:n.*74C>A
ENST00000584601.5:c.3405C>A	ENSP00000462438.1:p.Ala1135=
NM_001005862.2:c.3405C>A , LRG_724t1:c.3405C>A	NP_001005862.1:p.Ala1135=
NM_001289936.1:c.3450C>A , LRG_724t4:c.3450C>A	NP_001276865.1:p.Ala1150=
NM_001289937.1:c.*74C>A	NP_001276866.1:n.*74C>A
NM_004448.3:c.3495C>A , LRG_724t2:c.3495C>A	NP_004439.2:p.Ala1165=
NR_110535.1:n.3819C>A
XM_024450641.1:c.3633C>A	XP_024306409.1:p.Ala1211=
XM_024450642.1:c.3588C>A	XP_024306410.1:p.Ala1196=
XM_024450643.1:c.3543C>A	XP_024306411.1:p.Ala1181=
NM_001005862.3:c.3405C>A	NP_001005862.1:p.Ala1135=
NM_001289936.2:c.3450C>A	NP_001276865.1:p.Ala1150=
NM_001289937.2:c.*74C>A	NP_001276866.1:n.*74C>A
NM_001382782.1:c.3405C>A	NP_001369711.1:p.Ala1135=
NM_001382783.1:c.3405C>A	NP_001369712.1:p.Ala1135=
NM_001382784.1:c.3612C>A	NP_001369713.1:p.Ala1204=
NM_001382785.1:c.3597C>A	NP_001369714.1:p.Ala1199=
NM_001382786.1:c.3576C>A	NP_001369715.1:p.Ala1192=
NM_001382787.1:c.3570C>A	NP_001369716.1:p.Ala1190=
NM_001382788.1:c.3525C>A	NP_001369717.1:p.Ala1175=
NM_001382789.1:c.3516C>A	NP_001369718.1:p.Ala1172=
NM_001382790.1:c.3492C>A	NP_001369719.1:p.Ala1164=
NM_001382791.1:c.3486C>A	NP_001369720.1:p.Ala1162=
NM_001382792.1:c.3459C>A	NP_001369721.1:p.Ala1153=
NM_001382793.1:c.3453C>A	NP_001369722.1:p.Ala1151=
NM_001382794.1:c.3453C>A	NP_001369723.1:p.Ala1151=
NM_001382795.1:c.3447C>A	NP_001369724.1:p.Ala1149=
NM_001382796.1:c.3408C>A	NP_001369725.1:p.Ala1136=
NM_001382797.1:c.3396C>A	NP_001369726.1:p.Ala1132=
NM_001382798.1:c.3339C>A	NP_001369727.1:p.Ala1113=
NM_001382799.1:c.3315C>A	NP_001369728.1:p.Ala1105=
NM_001382800.1:c.3309C>A	NP_001369729.1:p.Ala1103=
NM_001382801.1:c.3291C>A	NP_001369730.1:p.Ala1097=
NM_001382802.1:c.3237C>A	NP_001369731.1:p.Ala1079=
NM_001382803.1:c.*74C>A	NP_001369732.1:n.*74C>A
NM_001382804.1:c.2667C>A	NP_001369733.1:p.Ala889=
NM_001382805.1:c.2544C>A	NP_001369734.1:p.Ala848=
NM_001382806.1:c.2457C>A	NP_001369735.1:p.Ala819=
NM_004448.4:c.3495C>A MANE Select	NP_004439.2:p.Ala1165=
NR_110535.2:n.3733C>A