Canonical Allele Identifier: CA499671622

Gene: ERBB2

Linked Data

• dbSNP Id: rs1597891618
• MyVariant Identifiers: chr17:g.37883616A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727363A>G , CM000679.2:g.39727363A>G	GRCh38
NC_000017.10:g.37883616A>G , CM000679.1:g.37883616A>G	GRCh37
NC_000017.9:g.35137142A>G	NCBI36
NG_007503.1:g.44224A>G , LRG_724:g.44224A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3228A>G MANE Select	ENSP00000269571.4:p.Ala1076=
ENST00000269571.9:c.3228A>G	ENSP00000269571.4:p.Ala1076=
ENST00000406381.6:c.3138A>G	ENSP00000385185.2:p.Ala1046=
ENST00000445658.6:c.2400A>G	ENSP00000404047.2:p.Ala800=
ENST00000541774.5:c.3183A>G	ENSP00000446466.1:p.Ala1061=
ENST00000578373.5:c.*3018A>G	ENSP00000463427.1:n.*3018A>G
ENST00000584450.5:c.3160-326A>G	ENSP00000463714.1:n.3160-326A>G
ENST00000584601.5:c.3138A>G	ENSP00000462438.1:p.Ala1046=
NM_001005862.2:c.3138A>G , LRG_724t1:c.3138A>G	NP_001005862.1:p.Ala1046=
NM_001289936.1:c.3183A>G , LRG_724t4:c.3183A>G	NP_001276865.1:p.Ala1061=
NM_001289937.1:c.3160-326A>G	NP_001276866.1:n.3160-326A>G
NM_004448.3:c.3228A>G , LRG_724t2:c.3228A>G	NP_004439.2:p.Ala1076=
NR_110535.1:n.3552A>G
XM_024450641.1:c.3366A>G	XP_024306409.1:p.Ala1122=
XM_024450642.1:c.3321A>G	XP_024306410.1:p.Ala1107=
XM_024450643.1:c.3276A>G	XP_024306411.1:p.Ala1092=
NM_001005862.3:c.3138A>G	NP_001005862.1:p.Ala1046=
NM_001289936.2:c.3183A>G	NP_001276865.1:p.Ala1061=
NM_001289937.2:c.3160-326A>G	NP_001276866.1:n.3160-326A>G
NM_001382782.1:c.3138A>G	NP_001369711.1:p.Ala1046=
NM_001382783.1:c.3138A>G	NP_001369712.1:p.Ala1046=
NM_001382784.1:c.3345A>G	NP_001369713.1:p.Ala1115=
NM_001382785.1:c.3330A>G	NP_001369714.1:p.Ala1110=
NM_001382786.1:c.3309A>G	NP_001369715.1:p.Ala1103=
NM_001382787.1:c.3303A>G	NP_001369716.1:p.Ala1101=
NM_001382788.1:c.3258A>G	NP_001369717.1:p.Ala1086=
NM_001382789.1:c.3249A>G	NP_001369718.1:p.Ala1083=
NM_001382790.1:c.3225A>G	NP_001369719.1:p.Ala1075=
NM_001382791.1:c.3219A>G	NP_001369720.1:p.Ala1073=
NM_001382792.1:c.3192A>G	NP_001369721.1:p.Ala1064=
NM_001382793.1:c.3186A>G	NP_001369722.1:p.Ala1062=
NM_001382794.1:c.3186A>G	NP_001369723.1:p.Ala1062=
NM_001382795.1:c.3180A>G	NP_001369724.1:p.Ala1060=
NM_001382796.1:c.3141A>G	NP_001369725.1:p.Ala1047=
NM_001382797.1:c.3129A>G	NP_001369726.1:p.Ala1043=
NM_001382798.1:c.3072A>G	NP_001369727.1:p.Ala1024=
NM_001382799.1:c.3048A>G	NP_001369728.1:p.Ala1016=
NM_001382800.1:c.3042A>G	NP_001369729.1:p.Ala1014=
NM_001382801.1:c.3024A>G	NP_001369730.1:p.Ala1008=
NM_001382802.1:c.2970A>G	NP_001369731.1:p.Ala990=
NM_001382803.1:c.3118-326A>G	NP_001369732.1:n.3118-326A>G
NM_001382804.1:c.2400A>G	NP_001369733.1:p.Ala800=
NM_001382805.1:c.2277A>G	NP_001369734.1:p.Ala759=
NM_001382806.1:c.2190A>G	NP_001369735.1:p.Ala730=
NM_004448.4:c.3228A>G MANE Select	NP_004439.2:p.Ala1076=
NR_110535.2:n.3466A>G