Canonical Allele Identifier: CA499671630

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883628G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727375G>A , CM000679.2:g.39727375G>A	GRCh38
NC_000017.10:g.37883628G>A , CM000679.1:g.37883628G>A	GRCh37
NC_000017.9:g.35137154G>A	NCBI36
NG_007503.1:g.44236G>A , LRG_724:g.44236G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3240G>A MANE Select	ENSP00000269571.4:p.Gly1080=
ENST00000269571.9:c.3240G>A	ENSP00000269571.4:p.Gly1080=
ENST00000406381.6:c.3150G>A	ENSP00000385185.2:p.Gly1050=
ENST00000445658.6:c.2412G>A	ENSP00000404047.2:p.Gly804=
ENST00000541774.5:c.3195G>A	ENSP00000446466.1:p.Gly1065=
ENST00000578373.5:c.*3030G>A	ENSP00000463427.1:n.*3030G>A
ENST00000584450.5:c.3160-314G>A	ENSP00000463714.1:n.3160-314G>A
ENST00000584601.5:c.3150G>A	ENSP00000462438.1:p.Gly1050=
NM_001005862.2:c.3150G>A , LRG_724t1:c.3150G>A	NP_001005862.1:p.Gly1050=
NM_001289936.1:c.3195G>A , LRG_724t4:c.3195G>A	NP_001276865.1:p.Gly1065=
NM_001289937.1:c.3160-314G>A	NP_001276866.1:n.3160-314G>A
NM_004448.3:c.3240G>A , LRG_724t2:c.3240G>A	NP_004439.2:p.Gly1080=
NR_110535.1:n.3564G>A
XM_024450641.1:c.3378G>A	XP_024306409.1:p.Gly1126=
XM_024450642.1:c.3333G>A	XP_024306410.1:p.Gly1111=
XM_024450643.1:c.3288G>A	XP_024306411.1:p.Gly1096=
NM_001005862.3:c.3150G>A	NP_001005862.1:p.Gly1050=
NM_001289936.2:c.3195G>A	NP_001276865.1:p.Gly1065=
NM_001289937.2:c.3160-314G>A	NP_001276866.1:n.3160-314G>A
NM_001382782.1:c.3150G>A	NP_001369711.1:p.Gly1050=
NM_001382783.1:c.3150G>A	NP_001369712.1:p.Gly1050=
NM_001382784.1:c.3357G>A	NP_001369713.1:p.Gly1119=
NM_001382785.1:c.3342G>A	NP_001369714.1:p.Gly1114=
NM_001382786.1:c.3321G>A	NP_001369715.1:p.Gly1107=
NM_001382787.1:c.3315G>A	NP_001369716.1:p.Gly1105=
NM_001382788.1:c.3270G>A	NP_001369717.1:p.Gly1090=
NM_001382789.1:c.3261G>A	NP_001369718.1:p.Gly1087=
NM_001382790.1:c.3237G>A	NP_001369719.1:p.Gly1079=
NM_001382791.1:c.3231G>A	NP_001369720.1:p.Gly1077=
NM_001382792.1:c.3204G>A	NP_001369721.1:p.Gly1068=
NM_001382793.1:c.3198G>A	NP_001369722.1:p.Gly1066=
NM_001382794.1:c.3198G>A	NP_001369723.1:p.Gly1066=
NM_001382795.1:c.3192G>A	NP_001369724.1:p.Gly1064=
NM_001382796.1:c.3153G>A	NP_001369725.1:p.Gly1051=
NM_001382797.1:c.3141G>A	NP_001369726.1:p.Gly1047=
NM_001382798.1:c.3084G>A	NP_001369727.1:p.Gly1028=
NM_001382799.1:c.3060G>A	NP_001369728.1:p.Gly1020=
NM_001382800.1:c.3054G>A	NP_001369729.1:p.Gly1018=
NM_001382801.1:c.3036G>A	NP_001369730.1:p.Gly1012=
NM_001382802.1:c.2982G>A	NP_001369731.1:p.Gly994=
NM_001382803.1:c.3118-314G>A	NP_001369732.1:n.3118-314G>A
NM_001382804.1:c.2412G>A	NP_001369733.1:p.Gly804=
NM_001382805.1:c.2289G>A	NP_001369734.1:p.Gly763=
NM_001382806.1:c.2202G>A	NP_001369735.1:p.Gly734=
NM_004448.4:c.3240G>A MANE Select	NP_004439.2:p.Gly1080=
NR_110535.2:n.3478G>A