Canonical Allele Identifier: CA399313239

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143296979
• MyVariant Identifiers: chr17:g.37884043A>C (hg19) ; chr17:g.39727790A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727790A>C , CM000679.2:g.39727790A>C	GRCh38
NC_000017.10:g.37884043A>C , CM000679.1:g.37884043A>C	GRCh37
NC_000017.9:g.35137569A>C	NCBI36
NG_007503.1:g.44651A>C , LRG_724:g.44651A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.3514A>C MANE Select	ENSP00000269571.4:p.Thr1172Pro
ENST00000269571.9:c.3514A>C	ENSP00000269571.4:p.Thr1172Pro
ENST00000406381.6:c.3424A>C	ENSP00000385185.2:p.Thr1142Pro
ENST00000445658.6:c.2686A>C	ENSP00000404047.2:p.Thr896Pro
ENST00000541774.5:c.3469A>C	ENSP00000446466.1:p.Thr1157Pro
ENST00000578373.5:c.*3304A>C	ENSP00000463427.1:n.*3304A>C
ENST00000584450.5:c.*93A>C	ENSP00000463714.1:n.*93A>C
ENST00000584601.5:c.3424A>C	ENSP00000462438.1:p.Thr1142Pro
NM_001005862.2:c.3424A>C , LRG_724t1:c.3424A>C	NP_001005862.1:p.Thr1142Pro
NM_001289936.1:c.3469A>C , LRG_724t4:c.3469A>C	NP_001276865.1:p.Thr1157Pro
NM_001289937.1:c.*93A>C	NP_001276866.1:n.*93A>C
NM_004448.3:c.3514A>C , LRG_724t2:c.3514A>C	NP_004439.2:p.Thr1172Pro
NR_110535.1:n.3838A>C
XM_024450641.1:c.3652A>C	XP_024306409.1:p.Thr1218Pro
XM_024450642.1:c.3607A>C	XP_024306410.1:p.Thr1203Pro
XM_024450643.1:c.3562A>C	XP_024306411.1:p.Thr1188Pro
NM_001005862.3:c.3424A>C	NP_001005862.1:p.Thr1142Pro
NM_001289936.2:c.3469A>C	NP_001276865.1:p.Thr1157Pro
NM_001289937.2:c.*93A>C	NP_001276866.1:n.*93A>C
NM_001382782.1:c.3424A>C	NP_001369711.1:p.Thr1142Pro
NM_001382783.1:c.3424A>C	NP_001369712.1:p.Thr1142Pro
NM_001382784.1:c.3631A>C	NP_001369713.1:p.Thr1211Pro
NM_001382785.1:c.3616A>C	NP_001369714.1:p.Thr1206Pro
NM_001382786.1:c.3595A>C	NP_001369715.1:p.Thr1199Pro
NM_001382787.1:c.3589A>C	NP_001369716.1:p.Thr1197Pro
NM_001382788.1:c.3544A>C	NP_001369717.1:p.Thr1182Pro
NM_001382789.1:c.3535A>C	NP_001369718.1:p.Thr1179Pro
NM_001382790.1:c.3511A>C	NP_001369719.1:p.Thr1171Pro
NM_001382791.1:c.3505A>C	NP_001369720.1:p.Thr1169Pro
NM_001382792.1:c.3478A>C	NP_001369721.1:p.Thr1160Pro
NM_001382793.1:c.3472A>C	NP_001369722.1:p.Thr1158Pro
NM_001382794.1:c.3472A>C	NP_001369723.1:p.Thr1158Pro
NM_001382795.1:c.3466A>C	NP_001369724.1:p.Thr1156Pro
NM_001382796.1:c.3427A>C	NP_001369725.1:p.Thr1143Pro
NM_001382797.1:c.3415A>C	NP_001369726.1:p.Thr1139Pro
NM_001382798.1:c.3358A>C	NP_001369727.1:p.Thr1120Pro
NM_001382799.1:c.3334A>C	NP_001369728.1:p.Thr1112Pro
NM_001382800.1:c.3328A>C	NP_001369729.1:p.Thr1110Pro
NM_001382801.1:c.3310A>C	NP_001369730.1:p.Thr1104Pro
NM_001382802.1:c.3256A>C	NP_001369731.1:p.Thr1086Pro
NM_001382803.1:c.*93A>C	NP_001369732.1:n.*93A>C
NM_001382804.1:c.2686A>C	NP_001369733.1:p.Thr896Pro
NM_001382805.1:c.2563A>C	NP_001369734.1:p.Thr855Pro
NM_001382806.1:c.2476A>C	NP_001369735.1:p.Thr826Pro
NM_004448.4:c.3514A>C MANE Select	NP_004439.2:p.Thr1172Pro
NR_110535.2:n.3752A>C