Canonical Allele Identifier: CA399313051

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39727760-C-A
• MyVariant Identifiers: chr17:g.37884013C>A (hg19) ; chr17:g.39727760C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727760C>A , CM000679.2:g.39727760C>A	GRCh38
NC_000017.10:g.37884013C>A , CM000679.1:g.37884013C>A	GRCh37
NC_000017.9:g.35137539C>A	NCBI36
NG_007503.1:g.44621C>A , LRG_724:g.44621C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3484C>A MANE Select	ENSP00000269571.4:p.Pro1162Thr
ENST00000269571.9:c.3484C>A	ENSP00000269571.4:p.Pro1162Thr
ENST00000406381.6:c.3394C>A	ENSP00000385185.2:p.Pro1132Thr
ENST00000445658.6:c.2656C>A	ENSP00000404047.2:p.Pro886Thr
ENST00000541774.5:c.3439C>A	ENSP00000446466.1:p.Pro1147Thr
ENST00000578373.5:c.*3274C>A	ENSP00000463427.1:n.*3274C>A
ENST00000584450.5:c.*63C>A	ENSP00000463714.1:n.*63C>A
ENST00000584601.5:c.3394C>A	ENSP00000462438.1:p.Pro1132Thr
NM_001005862.2:c.3394C>A , LRG_724t1:c.3394C>A	NP_001005862.1:p.Pro1132Thr
NM_001289936.1:c.3439C>A , LRG_724t4:c.3439C>A	NP_001276865.1:p.Pro1147Thr
NM_001289937.1:c.*63C>A	NP_001276866.1:n.*63C>A
NM_004448.3:c.3484C>A , LRG_724t2:c.3484C>A	NP_004439.2:p.Pro1162Thr
NR_110535.1:n.3808C>A
XM_024450641.1:c.3622C>A	XP_024306409.1:p.Pro1208Thr
XM_024450642.1:c.3577C>A	XP_024306410.1:p.Pro1193Thr
XM_024450643.1:c.3532C>A	XP_024306411.1:p.Pro1178Thr
NM_001005862.3:c.3394C>A	NP_001005862.1:p.Pro1132Thr
NM_001289936.2:c.3439C>A	NP_001276865.1:p.Pro1147Thr
NM_001289937.2:c.*63C>A	NP_001276866.1:n.*63C>A
NM_001382782.1:c.3394C>A	NP_001369711.1:p.Pro1132Thr
NM_001382783.1:c.3394C>A	NP_001369712.1:p.Pro1132Thr
NM_001382784.1:c.3601C>A	NP_001369713.1:p.Pro1201Thr
NM_001382785.1:c.3586C>A	NP_001369714.1:p.Pro1196Thr
NM_001382786.1:c.3565C>A	NP_001369715.1:p.Pro1189Thr
NM_001382787.1:c.3559C>A	NP_001369716.1:p.Pro1187Thr
NM_001382788.1:c.3514C>A	NP_001369717.1:p.Pro1172Thr
NM_001382789.1:c.3505C>A	NP_001369718.1:p.Pro1169Thr
NM_001382790.1:c.3481C>A	NP_001369719.1:p.Pro1161Thr
NM_001382791.1:c.3475C>A	NP_001369720.1:p.Pro1159Thr
NM_001382792.1:c.3448C>A	NP_001369721.1:p.Pro1150Thr
NM_001382793.1:c.3442C>A	NP_001369722.1:p.Pro1148Thr
NM_001382794.1:c.3442C>A	NP_001369723.1:p.Pro1148Thr
NM_001382795.1:c.3436C>A	NP_001369724.1:p.Pro1146Thr
NM_001382796.1:c.3397C>A	NP_001369725.1:p.Pro1133Thr
NM_001382797.1:c.3385C>A	NP_001369726.1:p.Pro1129Thr
NM_001382798.1:c.3328C>A	NP_001369727.1:p.Pro1110Thr
NM_001382799.1:c.3304C>A	NP_001369728.1:p.Pro1102Thr
NM_001382800.1:c.3298C>A	NP_001369729.1:p.Pro1100Thr
NM_001382801.1:c.3280C>A	NP_001369730.1:p.Pro1094Thr
NM_001382802.1:c.3226C>A	NP_001369731.1:p.Pro1076Thr
NM_001382803.1:c.*63C>A	NP_001369732.1:n.*63C>A
NM_001382804.1:c.2656C>A	NP_001369733.1:p.Pro886Thr
NM_001382805.1:c.2533C>A	NP_001369734.1:p.Pro845Thr
NM_001382806.1:c.2446C>A	NP_001369735.1:p.Pro816Thr
NM_004448.4:c.3484C>A MANE Select	NP_004439.2:p.Pro1162Thr
NR_110535.2:n.3722C>A