Canonical Allele Identifier: CA399314373

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884193T>C (hg19) ; chr17:g.39727940T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727940T>C , CM000679.2:g.39727940T>C	GRCh38
NC_000017.10:g.37884193T>C , CM000679.1:g.37884193T>C	GRCh37
NC_000017.9:g.35137719T>C	NCBI36
NG_007503.1:g.44801T>C , LRG_724:g.44801T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3664T>C MANE Select	ENSP00000269571.4:p.Tyr1222His
ENST00000269571.9:c.3664T>C	ENSP00000269571.4:p.Tyr1222His
ENST00000406381.6:c.3574T>C	ENSP00000385185.2:p.Tyr1192His
ENST00000445658.6:c.2836T>C	ENSP00000404047.2:p.Tyr946His
ENST00000541774.5:c.3619T>C	ENSP00000446466.1:p.Tyr1207His
ENST00000578373.5:c.*3454T>C	ENSP00000463427.1:n.*3454T>C
ENST00000584450.5:c.*243T>C	ENSP00000463714.1:n.*243T>C
ENST00000584601.5:c.3574T>C	ENSP00000462438.1:p.Tyr1192His
NM_001005862.2:c.3574T>C , LRG_724t1:c.3574T>C	NP_001005862.1:p.Tyr1192His
NM_001289936.1:c.3619T>C , LRG_724t4:c.3619T>C	NP_001276865.1:p.Tyr1207His
NM_001289937.1:c.*243T>C	NP_001276866.1:n.*243T>C
NM_004448.3:c.3664T>C , LRG_724t2:c.3664T>C	NP_004439.2:p.Tyr1222His
NR_110535.1:n.3988T>C
XM_024450641.1:c.3802T>C	XP_024306409.1:p.Tyr1268His
XM_024450642.1:c.3757T>C	XP_024306410.1:p.Tyr1253His
XM_024450643.1:c.3712T>C	XP_024306411.1:p.Tyr1238His
NM_001005862.3:c.3574T>C	NP_001005862.1:p.Tyr1192His
NM_001289936.2:c.3619T>C	NP_001276865.1:p.Tyr1207His
NM_001289937.2:c.*243T>C	NP_001276866.1:n.*243T>C
NM_001382782.1:c.3574T>C	NP_001369711.1:p.Tyr1192His
NM_001382783.1:c.3574T>C	NP_001369712.1:p.Tyr1192His
NM_001382784.1:c.3781T>C	NP_001369713.1:p.Tyr1261His
NM_001382785.1:c.3766T>C	NP_001369714.1:p.Tyr1256His
NM_001382786.1:c.3745T>C	NP_001369715.1:p.Tyr1249His
NM_001382787.1:c.3739T>C	NP_001369716.1:p.Tyr1247His
NM_001382788.1:c.3694T>C	NP_001369717.1:p.Tyr1232His
NM_001382789.1:c.3685T>C	NP_001369718.1:p.Tyr1229His
NM_001382790.1:c.3661T>C	NP_001369719.1:p.Tyr1221His
NM_001382791.1:c.3655T>C	NP_001369720.1:p.Tyr1219His
NM_001382792.1:c.3628T>C	NP_001369721.1:p.Tyr1210His
NM_001382793.1:c.3622T>C	NP_001369722.1:p.Tyr1208His
NM_001382794.1:c.3622T>C	NP_001369723.1:p.Tyr1208His
NM_001382795.1:c.3616T>C	NP_001369724.1:p.Tyr1206His
NM_001382796.1:c.3577T>C	NP_001369725.1:p.Tyr1193His
NM_001382797.1:c.3565T>C	NP_001369726.1:p.Tyr1189His
NM_001382798.1:c.3508T>C	NP_001369727.1:p.Tyr1170His
NM_001382799.1:c.3484T>C	NP_001369728.1:p.Tyr1162His
NM_001382800.1:c.3478T>C	NP_001369729.1:p.Tyr1160His
NM_001382801.1:c.3460T>C	NP_001369730.1:p.Tyr1154His
NM_001382802.1:c.3406T>C	NP_001369731.1:p.Tyr1136His
NM_001382803.1:c.*243T>C	NP_001369732.1:n.*243T>C
NM_001382804.1:c.2836T>C	NP_001369733.1:p.Tyr946His
NM_001382805.1:c.2713T>C	NP_001369734.1:p.Tyr905His
NM_001382806.1:c.2626T>C	NP_001369735.1:p.Tyr876His
NM_004448.4:c.3664T>C MANE Select	NP_004439.2:p.Tyr1222His
NR_110535.2:n.3902T>C