Canonical Allele Identifier: CA499890833

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884162T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727909T>G , CM000679.2:g.39727909T>G	GRCh38
NC_000017.10:g.37884162T>G , CM000679.1:g.37884162T>G	GRCh37
NC_000017.9:g.35137688T>G	NCBI36
NG_007503.1:g.44770T>G , LRG_724:g.44770T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3633T>G MANE Select	ENSP00000269571.4:p.Pro1211=
ENST00000269571.9:c.3633T>G	ENSP00000269571.4:p.Pro1211=
ENST00000406381.6:c.3543T>G	ENSP00000385185.2:p.Pro1181=
ENST00000445658.6:c.2805T>G	ENSP00000404047.2:p.Pro935=
ENST00000541774.5:c.3588T>G	ENSP00000446466.1:p.Pro1196=
ENST00000578373.5:c.*3423T>G	ENSP00000463427.1:n.*3423T>G
ENST00000584450.5:c.*212T>G	ENSP00000463714.1:n.*212T>G
ENST00000584601.5:c.3543T>G	ENSP00000462438.1:p.Pro1181=
NM_001005862.2:c.3543T>G , LRG_724t1:c.3543T>G	NP_001005862.1:p.Pro1181=
NM_001289936.1:c.3588T>G , LRG_724t4:c.3588T>G	NP_001276865.1:p.Pro1196=
NM_001289937.1:c.*212T>G	NP_001276866.1:n.*212T>G
NM_004448.3:c.3633T>G , LRG_724t2:c.3633T>G	NP_004439.2:p.Pro1211=
NR_110535.1:n.3957T>G
XM_024450641.1:c.3771T>G	XP_024306409.1:p.Pro1257=
XM_024450642.1:c.3726T>G	XP_024306410.1:p.Pro1242=
XM_024450643.1:c.3681T>G	XP_024306411.1:p.Pro1227=
NM_001005862.3:c.3543T>G	NP_001005862.1:p.Pro1181=
NM_001289936.2:c.3588T>G	NP_001276865.1:p.Pro1196=
NM_001289937.2:c.*212T>G	NP_001276866.1:n.*212T>G
NM_001382782.1:c.3543T>G	NP_001369711.1:p.Pro1181=
NM_001382783.1:c.3543T>G	NP_001369712.1:p.Pro1181=
NM_001382784.1:c.3750T>G	NP_001369713.1:p.Pro1250=
NM_001382785.1:c.3735T>G	NP_001369714.1:p.Pro1245=
NM_001382786.1:c.3714T>G	NP_001369715.1:p.Pro1238=
NM_001382787.1:c.3708T>G	NP_001369716.1:p.Pro1236=
NM_001382788.1:c.3663T>G	NP_001369717.1:p.Pro1221=
NM_001382789.1:c.3654T>G	NP_001369718.1:p.Pro1218=
NM_001382790.1:c.3630T>G	NP_001369719.1:p.Pro1210=
NM_001382791.1:c.3624T>G	NP_001369720.1:p.Pro1208=
NM_001382792.1:c.3597T>G	NP_001369721.1:p.Pro1199=
NM_001382793.1:c.3591T>G	NP_001369722.1:p.Pro1197=
NM_001382794.1:c.3591T>G	NP_001369723.1:p.Pro1197=
NM_001382795.1:c.3585T>G	NP_001369724.1:p.Pro1195=
NM_001382796.1:c.3546T>G	NP_001369725.1:p.Pro1182=
NM_001382797.1:c.3534T>G	NP_001369726.1:p.Pro1178=
NM_001382798.1:c.3477T>G	NP_001369727.1:p.Pro1159=
NM_001382799.1:c.3453T>G	NP_001369728.1:p.Pro1151=
NM_001382800.1:c.3447T>G	NP_001369729.1:p.Pro1149=
NM_001382801.1:c.3429T>G	NP_001369730.1:p.Pro1143=
NM_001382802.1:c.3375T>G	NP_001369731.1:p.Pro1125=
NM_001382803.1:c.*212T>G	NP_001369732.1:n.*212T>G
NM_001382804.1:c.2805T>G	NP_001369733.1:p.Pro935=
NM_001382805.1:c.2682T>G	NP_001369734.1:p.Pro894=
NM_001382806.1:c.2595T>G	NP_001369735.1:p.Pro865=
NM_004448.4:c.3633T>G MANE Select	NP_004439.2:p.Pro1211=
NR_110535.2:n.3871T>G