Canonical Allele Identifier: CA499671658

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883670A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727417A>C , CM000679.2:g.39727417A>C	GRCh38
NC_000017.10:g.37883670A>C , CM000679.1:g.37883670A>C	GRCh37
NC_000017.9:g.35137196A>C	NCBI36
NG_007503.1:g.44278A>C , LRG_724:g.44278A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3282A>C MANE Select	ENSP00000269571.4:p.Ala1094=
ENST00000269571.9:c.3282A>C	ENSP00000269571.4:p.Ala1094=
ENST00000406381.6:c.3192A>C	ENSP00000385185.2:p.Ala1064=
ENST00000445658.6:c.2454A>C	ENSP00000404047.2:p.Ala818=
ENST00000541774.5:c.3237A>C	ENSP00000446466.1:p.Ala1079=
ENST00000578373.5:c.*3072A>C	ENSP00000463427.1:n.*3072A>C
ENST00000584450.5:c.3160-272A>C	ENSP00000463714.1:n.3160-272A>C
ENST00000584601.5:c.3192A>C	ENSP00000462438.1:p.Ala1064=
NM_001005862.2:c.3192A>C , LRG_724t1:c.3192A>C	NP_001005862.1:p.Ala1064=
NM_001289936.1:c.3237A>C , LRG_724t4:c.3237A>C	NP_001276865.1:p.Ala1079=
NM_001289937.1:c.3160-272A>C	NP_001276866.1:n.3160-272A>C
NM_004448.3:c.3282A>C , LRG_724t2:c.3282A>C	NP_004439.2:p.Ala1094=
NR_110535.1:n.3606A>C
XM_024450641.1:c.3420A>C	XP_024306409.1:p.Ala1140=
XM_024450642.1:c.3375A>C	XP_024306410.1:p.Ala1125=
XM_024450643.1:c.3330A>C	XP_024306411.1:p.Ala1110=
NM_001005862.3:c.3192A>C	NP_001005862.1:p.Ala1064=
NM_001289936.2:c.3237A>C	NP_001276865.1:p.Ala1079=
NM_001289937.2:c.3160-272A>C	NP_001276866.1:n.3160-272A>C
NM_001382782.1:c.3192A>C	NP_001369711.1:p.Ala1064=
NM_001382783.1:c.3192A>C	NP_001369712.1:p.Ala1064=
NM_001382784.1:c.3399A>C	NP_001369713.1:p.Ala1133=
NM_001382785.1:c.3384A>C	NP_001369714.1:p.Ala1128=
NM_001382786.1:c.3363A>C	NP_001369715.1:p.Ala1121=
NM_001382787.1:c.3357A>C	NP_001369716.1:p.Ala1119=
NM_001382788.1:c.3312A>C	NP_001369717.1:p.Ala1104=
NM_001382789.1:c.3303A>C	NP_001369718.1:p.Ala1101=
NM_001382790.1:c.3279A>C	NP_001369719.1:p.Ala1093=
NM_001382791.1:c.3273A>C	NP_001369720.1:p.Ala1091=
NM_001382792.1:c.3246A>C	NP_001369721.1:p.Ala1082=
NM_001382793.1:c.3240A>C	NP_001369722.1:p.Ala1080=
NM_001382794.1:c.3240A>C	NP_001369723.1:p.Ala1080=
NM_001382795.1:c.3234A>C	NP_001369724.1:p.Ala1078=
NM_001382796.1:c.3195A>C	NP_001369725.1:p.Ala1065=
NM_001382797.1:c.3183A>C	NP_001369726.1:p.Ala1061=
NM_001382798.1:c.3126A>C	NP_001369727.1:p.Ala1042=
NM_001382799.1:c.3102A>C	NP_001369728.1:p.Ala1034=
NM_001382800.1:c.3096A>C	NP_001369729.1:p.Ala1032=
NM_001382801.1:c.3078A>C	NP_001369730.1:p.Ala1026=
NM_001382802.1:c.3024A>C	NP_001369731.1:p.Ala1008=
NM_001382803.1:c.3118-272A>C	NP_001369732.1:n.3118-272A>C
NM_001382804.1:c.2454A>C	NP_001369733.1:p.Ala818=
NM_001382805.1:c.2331A>C	NP_001369734.1:p.Ala777=
NM_001382806.1:c.2244A>C	NP_001369735.1:p.Ala748=
NM_004448.4:c.3282A>C MANE Select	NP_004439.2:p.Ala1094=
NR_110535.2:n.3520A>C