Canonical Allele Identifier: CA499671598

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883586T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727333T>C , CM000679.2:g.39727333T>C	GRCh38
NC_000017.10:g.37883586T>C , CM000679.1:g.37883586T>C	GRCh37
NC_000017.9:g.35137112T>C	NCBI36
NG_007503.1:g.44194T>C , LRG_724:g.44194T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3198T>C MANE Select	ENSP00000269571.4:p.Ser1066=
ENST00000269571.9:c.3198T>C	ENSP00000269571.4:p.Ser1066=
ENST00000406381.6:c.3108T>C	ENSP00000385185.2:p.Ser1036=
ENST00000445658.6:c.2370T>C	ENSP00000404047.2:p.Ser790=
ENST00000541774.5:c.3153T>C	ENSP00000446466.1:p.Ser1051=
ENST00000578373.5:c.*2988T>C	ENSP00000463427.1:n.*2988T>C
ENST00000584450.5:c.3159+330T>C	ENSP00000463714.1:n.3159+330T>C
ENST00000584601.5:c.3108T>C	ENSP00000462438.1:p.Ser1036=
NM_001005862.2:c.3108T>C , LRG_724t1:c.3108T>C	NP_001005862.1:p.Ser1036=
NM_001289936.1:c.3153T>C , LRG_724t4:c.3153T>C	NP_001276865.1:p.Ser1051=
NM_001289937.1:c.3159+330T>C	NP_001276866.1:n.3159+330T>C
NM_004448.3:c.3198T>C , LRG_724t2:c.3198T>C	NP_004439.2:p.Ser1066=
NR_110535.1:n.3522T>C
XM_024450641.1:c.3336T>C	XP_024306409.1:p.Ser1112=
XM_024450642.1:c.3291T>C	XP_024306410.1:p.Ser1097=
XM_024450643.1:c.3246T>C	XP_024306411.1:p.Ser1082=
NM_001005862.3:c.3108T>C	NP_001005862.1:p.Ser1036=
NM_001289936.2:c.3153T>C	NP_001276865.1:p.Ser1051=
NM_001289937.2:c.3159+330T>C	NP_001276866.1:n.3159+330T>C
NM_001382782.1:c.3108T>C	NP_001369711.1:p.Ser1036=
NM_001382783.1:c.3108T>C	NP_001369712.1:p.Ser1036=
NM_001382784.1:c.3315T>C	NP_001369713.1:p.Ser1105=
NM_001382785.1:c.3300T>C	NP_001369714.1:p.Ser1100=
NM_001382786.1:c.3279T>C	NP_001369715.1:p.Ser1093=
NM_001382787.1:c.3273T>C	NP_001369716.1:p.Ser1091=
NM_001382788.1:c.3228T>C	NP_001369717.1:p.Ser1076=
NM_001382789.1:c.3219T>C	NP_001369718.1:p.Ser1073=
NM_001382790.1:c.3195T>C	NP_001369719.1:p.Ser1065=
NM_001382791.1:c.3189T>C	NP_001369720.1:p.Ser1063=
NM_001382792.1:c.3162T>C	NP_001369721.1:p.Ser1054=
NM_001382793.1:c.3156T>C	NP_001369722.1:p.Ser1052=
NM_001382794.1:c.3156T>C	NP_001369723.1:p.Ser1052=
NM_001382795.1:c.3150T>C	NP_001369724.1:p.Ser1050=
NM_001382796.1:c.3111T>C	NP_001369725.1:p.Ser1037=
NM_001382797.1:c.3099T>C	NP_001369726.1:p.Ser1033=
NM_001382798.1:c.3042T>C	NP_001369727.1:p.Ser1014=
NM_001382799.1:c.3018T>C	NP_001369728.1:p.Ser1006=
NM_001382800.1:c.3012T>C	NP_001369729.1:p.Ser1004=
NM_001382801.1:c.2994T>C	NP_001369730.1:p.Ser998=
NM_001382802.1:c.2940T>C	NP_001369731.1:p.Ser980=
NM_001382803.1:c.3117+330T>C	NP_001369732.1:n.3117+330T>C
NM_001382804.1:c.2370T>C	NP_001369733.1:p.Ser790=
NM_001382805.1:c.2247T>C	NP_001369734.1:p.Ser749=
NM_001382806.1:c.2160T>C	NP_001369735.1:p.Ser720=
NM_004448.4:c.3198T>C MANE Select	NP_004439.2:p.Ser1066=
NR_110535.2:n.3436T>C